U.S. flag

An official website of the United States government

nsv6917693

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:350,362

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 883 SVs from 74 studies. See in: genome view    
    Submitted genomic56,149,374-56,499,735Question Mark
    Overlapping variant regions from other studies: 885 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):55,916,850-56,267,211Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6917693Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1156,149,37456,499,735
    nsv6917693RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1155,916,85056,267,211

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351656deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351656Submitted genomicNC_000011.10:g.561
    49374_56499735del
    GRCh38 (hg38)NC_000011.10Chr1156,149,37456,499,735
    nssv18351656RemappedPerfectNC_000011.9:g.5591
    6850_56267211del
    GRCh37.p13First PassNC_000011.9Chr1155,916,85056,267,211

    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)
    nssv183516561.1e-053267668
    Support Center