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nsv6905813

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:387,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1266 SVs from 95 studies. See in: genome view    
    Submitted genomic67,694,101-68,081,300Question Mark
    Overlapping variant regions from other studies: 1264 SVs from 95 studies. See in: genome view    
    Remapped(Score: Good):67,461,572-67,848,767Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6905813Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1167,694,10168,081,300
    nsv6905813RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,461,57267,848,767

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353129deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353129Submitted genomicNC_000011.10:g.676
    94101_68081300del
    GRCh38 (hg38)NC_000011.10Chr1167,694,10168,081,300
    nssv18353129RemappedGoodNC_000011.9:g.6746
    1572_67848767del
    GRCh37.p13First PassNC_000011.9Chr1167,461,57267,848,767

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv183531290.002523253190
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