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nsv6962409

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,574

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 26 studies. See in: genome view    
    Submitted genomic70,655,252-70,657,825Question Mark
    Overlapping variant regions from other studies: 84 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):71,121,969-71,124,542Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6962409Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1470,655,25270,657,825
    nsv6962409RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1471,121,96971,124,542

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18389443deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18389443Submitted genomicNC_000014.9:g.7065
    5252_70657825del
    GRCh38 (hg38)NC_000014.9Chr1470,655,25270,657,825
    nssv18389443RemappedPerfectNC_000014.8:g.7112
    1969_71124542del
    GRCh37.p13First PassNC_000014.8Chr1471,121,96971,124,542

    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)
    nssv18389443<0.001115252492
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