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nsv6966448

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:148,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 498 SVs from 55 studies. See in: genome view    
    Submitted genomic40,764,501-40,912,500Question Mark
    Overlapping variant regions from other studies: 498 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):41,056,699-41,204,698Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6966448Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1540,764,50140,912,500
    nsv6966448RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,056,69941,204,698

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18619339duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18619339Submitted genomicNC_000015.10:g.407
    64501_40912500dup
    GRCh38 (hg38)NC_000015.10Chr1540,764,50140,912,500
    nssv18619339RemappedPerfectNC_000015.9:g.4105
    6699_41204698dup
    GRCh37.p13First PassNC_000015.9Chr1541,056,69941,204,698

    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)
    nssv186193394e-061275746
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