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nsv6958871

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:182

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 19 studies. See in: genome view    
    Submitted genomic103,914,992-103,915,173Question Mark
    Overlapping variant regions from other studies: 128 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):104,381,329-104,381,510Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6958871Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14103,914,992103,915,173
    nsv6958871RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14104,381,329104,381,510

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18612972duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18612972Submitted genomicNC_000014.9:g.1039
    14992_103915173dup
    GRCh38 (hg38)NC_000014.9Chr14103,914,992103,915,173
    nssv18612972RemappedPerfectNC_000014.8:g.1043
    81329_104381510dup
    GRCh37.p13First PassNC_000014.8Chr14104,381,329104,381,510

    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)
    nssv186129723.4e-058227240
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