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nsv6911508

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:510,372

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1774 SVs from 99 studies. See in: genome view    
    Submitted genomic67,541,590-68,051,961Question Mark
    Overlapping variant regions from other studies: 1772 SVs from 99 studies. See in: genome view    
    Remapped(Score: Good):67,309,061-67,819,428Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6911508Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1167,541,59068,051,961
    nsv6911508RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,309,06167,819,428

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18587668duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18587668Submitted genomicNC_000011.10:g.675
    41590_68051961dup
    GRCh38 (hg38)NC_000011.10Chr1167,541,59068,051,961
    nssv18587668RemappedGoodNC_000011.9:g.6730
    9061_67819428dup
    GRCh37.p13First PassNC_000011.9Chr1167,309,06167,819,428

    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)
    nssv185876684e-061274260
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