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nsv6761607

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,942

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 36 studies. See in: genome view    
    Submitted genomic79,265,049-79,269,990Question Mark
    Overlapping variant regions from other studies: 141 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):78,560,872-78,565,813Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6761607Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr579,265,04979,269,990
    nsv6761607RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr578,560,87278,565,813

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18517809deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18517809Submitted genomicNC_000005.10:g.792
    65049_79269990del
    GRCh38 (hg38)NC_000005.10Chr579,265,04979,269,990
    nssv18517809RemappedPerfectNC_000005.9:g.7856
    0872_78565813del
    GRCh37.p13First PassNC_000005.9Chr578,560,87278,565,813

    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)
    nssv185178091.8e-055274894
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