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nsv6974443

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,617

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 30 studies. See in: genome view    
    Submitted genomic92,689,488-92,700,104Question Mark
    Overlapping variant regions from other studies: 109 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):93,155,833-93,166,449Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6974443Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1492,689,48892,700,104
    nsv6974443RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1493,155,83393,166,449

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18391607deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18391607Submitted genomicNC_000014.9:g.9268
    9488_92700104del
    GRCh38 (hg38)NC_000014.9Chr1492,689,48892,700,104
    nssv18391607RemappedPerfectNC_000014.8:g.9315
    5833_93166449del
    GRCh37.p13First PassNC_000014.8Chr1493,155,83393,166,449

    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)
    nssv183916074e-061276242
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