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nsv6763798

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:773,395

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1635 SVs from 86 studies. See in: genome view    
    Submitted genomic111,959,103-112,732,497Question Mark
    Overlapping variant regions from other studies: 1635 SVs from 86 studies. See in: genome view    
    Remapped(Score: Perfect):111,294,800-112,068,194Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6763798Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5111,959,103112,732,497
    nsv6763798RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5111,294,800112,068,194

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18693159duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18693159Submitted genomicNC_000005.10:g.111
    959103_112732497du
    p
    GRCh38 (hg38)NC_000005.10Chr5111,959,103112,732,497
    nssv18693159RemappedPerfectNC_000005.9:g.1112
    94800_112068194dup
    GRCh37.p13First PassNC_000005.9Chr5111,294,800112,068,194

    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)
    nssv186931594e-061272192
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