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mtDNA · Maternal lineage

N9B2

mtDNA Haplogroup N9B2

A reference profile for one lineage branch. Shared haplogroups do not establish a family relationship or cultural identity.

Reference profile

Branch background

Historical context for mtDNA lineage branch N9B2

Origins and Evolution

mtDNA haplogroup N9B2 is a descendant subclade of N9B, itself part of the broader East Asian macro-haplogroup N9. N9B has been strongly associated with the Late Upper Paleolithic and Early Holocene populations of the Japanese archipelago (notably Jomon-era remains) and nearby northeastern Asian coastal populations. N9B2 likely formed after the initial diversification of N9B, in the early Holocene (roughly around 10 kya by molecular-clock inference), representing a more derived maternal lineage that rose within local hunter-gatherer populations in or near the Japanese islands and adjacent coastal continental regions.

The estimated age for N9B2 is younger than the parent N9B (commonly dated ~18 kya), consistent with a split occurring during the climatic and demographic shifts at the Pleistocene–Holocene transition, when regional populations experienced isolation, local differentiation, and localized expansions.

Subclades

N9B2 is itself a sub-branch within the N9B clade; depending on the resolution of complete mtDNA sequencing in available samples, N9B2 may contain further downstream sublineages observed at low frequency. High-resolution phylogenies built from whole-mitogenome data are necessary to resolve additional internal structure (naming such downstream branches as N9B2a, N9B2b, etc., if supported). As with many regionally restricted mtDNA clades, sampling density drives discovery of subclades, so future ancient and modern mitogenomes from Japan and coastal Northeast Asia may reveal further diversification.

Geographical Distribution

N9B2 is concentrated in the Japanese archipelago, with its highest representation among populations and ancient remains from Hokkaido, northern Honshu (Tōhoku), and the Ryukyu islands, reflecting continuity with Jomon-period maternal lineages. It also appears sporadically among indigenous groups of the Russian Far East (coastal Siberia), such as populations historically present along the Sea of Okhotsk and lower Amur, and at low frequencies in mainland East Asian groups (Koreans, Han Chinese) and isolated cases in Southeast Asia and Central Asia attributable to later mobility.

Overall, the distribution pattern indicates a strong northeastern East Asian/japano-centric focus with decreasing frequencies moving outward from the archipelago.

Historical and Cultural Significance

Because of its geographic pattern, N9B2 is of particular interest for studies of Jomon-period population structure and maternal continuity. The clade helps trace maternal ancestry that persisted in insular Japan through the Holocene and is enriched among groups with elevated indigenous ancestry (e.g., Ainu, some Ryukyuan lineages). N9B2 therefore contributes to reconstructing peopling scenarios in which Late Pleistocene/Early Holocene hunter-gatherer communities in the archipelago maintained genetic continuity while later agricultural migrations (e.g., Yayoi-associated) introduced new maternal lineages and altered frequency profiles.

Findings of N9B2 or closely related N9B lineages in coastal Siberian contexts also support prehistoric interaction along the northwest Pacific coast, consistent with archaeological evidence for maritime adaptation and episodic gene flow between islands and the mainland.

Conclusion

mtDNA N9B2 is a derived, regionally focused maternal lineage nested within N9B that documents aspects of maternal population history in northeastern East Asia and Japan during the early Holocene. While currently observed at low to moderate frequencies, particularly in northern and insular Japanese populations and some coastal Siberian groups, increased sampling of ancient and modern whole mitogenomes may clarify its internal diversity, age estimates, and precise role in postglacial population dynamics of the northwest Pacific.

Key Points

  • Origins and Evolution
  • Subclades
  • Geographical Distribution
  • Historical and Cultural Significance
  • Conclusion
Reference profile

Tree & Relationships

Phylogenetic context and subclades

Evolution Path

Follow the recorded parent branches toward N9B2. Dates are estimates and can change as reference data is revised.

Steps Haplogroup Age Estimate Archaeology Era Time Passed Immediate Descendants Tested Modern Descendants Ancient Connections
1 N9B2 Current ~10,000 years ago Neolithic 10,000 years 1 0 0
2 N9B ~18,000 years ago Mesolithic 18,000 years 3 0 21
3 N9 ~25,000 years ago Paleolithic 25,000 years 3 178 0
4 N ~60,000 years ago Paleolithic 60,000 years 16 26,150 13
5 L3 ~70,000 years ago Paleolithic 70,000 years 7 30,162 6
6 L3'4 - - - 2 30,212 0
7 L3'4'6 - - - 2 30,216 0
8 L2'3'4'6 - - - 2 31,333 0
9 L2'3'4'5'6'7 - - - 2 31,349 0
10 L1'2'3'4'5'6'7 - - - 2 31,852 0
11 L ~160,000 years ago Paleolithic 160,000 years 2 32,236 5

Siblings (2)

Other branches from the same parent haplogroup

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Where in the World

Geographic distribution and modern presence

Recorded origin

Northeast/East Asia (Japanese archipelago region)

Modern Distribution

The populations where mtDNA haplogroup N9B2 is found include:

  1. Japanese populations (notably in Hokkaido, Tohoku, and Ryukyu/Okinawa regions)
  2. Ancient Jomon-era remains from the Japanese archipelago
  3. Ainu and Ryukyuan-related modern groups with elevated indigenous maternal ancestry
  4. Koreans and some Northeast Asian mainland populations (lower frequencies)
  5. Indigenous peoples of the Russian Far East / coastal Siberia (e.g., Nivkh, Ulchi; sporadic occurrences)
  6. Han Chinese and other East Asian populations at low frequencies
  7. Southeast Asian populations (rare and localized occurrences)
  8. Central Asian and West Eurasian occurrences that are generally rare and attributable to later or sparse prehistoric gene flow
  9. Modern urban and mixed populations across East and Southeast Asia due to recent admixture
Historical context

A branch through time

Estimated formation in a broad historical timeline. Period markers provide context and do not imply a connection with particular cultures.

  1. ~10k years ago

    Neolithic Revolution

    Agriculture begins, settled communities form

  2. ~10k years ago

    Haplogroup N9B2

    Estimated formation of this mtDNA branch; dates and locations are reference estimates.

    This branch
  3. ~5k years ago

    Bronze Age

    Metalworking, writing, and early civilizations

  4. ~3k years ago

    Iron Age

    Iron tools, expanded trade networks

  5. ~2.5k years ago

    Classical Antiquity

    Greek and Roman civilizations flourish

  6. Present

    Present Day

    Modern era

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Archaeological context

Recorded archaeological associations for mtDNA branch N9B2

Recorded associations

These labels describe archaeological contexts recorded for reference samples linked to N9B2. An association does not establish that all carriers belonged to a culture or followed a particular migration route.

Early Jomon Initial Jomon Jomon
Culture assignments are based on archaeological context of ancient DNA samples and may represent regional associations during specific time periods.
Reference profile

Sample Catalog

1 subclade carrier of haplogroup N9B2 (no direct carriers in the current reference selection)

1 shown · 1 matching samples

Portraits are AI-generated illustrations. Sample labels and accession IDs identify the reference records.

Portrait Sample Country Era Date Culture mtDNA Match
AI-generated illustrative portrait of Chiba HG Jomon individual, Rokutsu Shell Mound, Japan (984-835 BCE)
Sample ID: I13883
Japan Jomon Period Japan 984-835 calBCE (2770±20 BP, PSUAMS-7943) Jomon N9b2a Subclade
MATERNAL LINEAGE · ANCIENT DNA

Ancient lineage evidence map

Follow parent clades toward this branch and explore where ancient carriers were found.

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Markers are archaeological find locations. A dashed connector is an uncertain, proposed geographic transition between consecutive branches supported by multiple dated observations; it is not an exact travel route, birthplace or proof of direct descent. Parent-clade samples may belong to other descendant branches. Gaps remain where evidence is insufficient. Sample dates differ from haplogroup formation dates.

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Carrier Distribution Map

Geographic distribution of 1 ancient DNA sample (direct and subclade carriers of N9B2)

Subclade carrier
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Temporal Distribution

Distribution of carriers across archaeological periods

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Geographic Distribution

Counts by recorded sample country. These reflect the available reference selection, not population frequencies.

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Country × Era Distribution

Compare recorded sample counts across countries and archaeological periods. Select a populated cell to inspect a sample.

Data

Data & Provenance

Source information and data quality

Last Updated 2026-02-16
Confidence Score 50/100
Coverage Low

Data Source

Classification, estimated dates and geographic context reflect the recorded reference data and may change as evidence is revised. Sample coverage is uneven; recorded locations and archaeological associations do not establish personal origin or cultural identity.