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nsv6974587

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:223,628

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 997 SVs from 71 studies. See in: genome view    
    Submitted genomic102,488,906-102,712,533Question Mark
    Overlapping variant regions from other studies: 997 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):102,955,243-103,178,870Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6974587Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14102,488,906102,712,533
    nsv6974587RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14102,955,243103,178,870

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18612887duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18612887Submitted genomicNC_000014.9:g.1024
    88906_102712533dup
    GRCh38 (hg38)NC_000014.9Chr14102,488,906102,712,533
    nssv18612887RemappedPerfectNC_000014.8:g.1029
    55243_103178870dup
    GRCh37.p13First PassNC_000014.8Chr14102,955,243103,178,870

    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)
    nssv186128874e-061274268
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