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nsv7057741

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:167,485

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 558 SVs from 70 studies. See in: genome view    
    Submitted genomic80,473,429-80,640,913Question Mark
    Overlapping variant regions from other studies: 558 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):80,102,745-80,270,229Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057741Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr780,473,42980,640,913
    nsv7057741RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr780,102,74580,270,229

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782014inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782014Submitted genomicNC_000007.14:g.804
    73429_80640913inv
    GRCh38 (hg38)NC_000007.14Chr780,473,42980,640,913
    nssv18782014RemappedPerfectNC_000007.13:g.801
    02745_80270229inv
    GRCh37.p13First PassNC_000007.13Chr780,102,74580,270,229

    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)
    nssv187820144e-061276268
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