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nsv6970821

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:234,295

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 665 SVs from 71 studies. See in: genome view    
    Submitted genomic101,391,345-101,625,639Question Mark
    Overlapping variant regions from other studies: 665 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):101,857,682-102,091,976Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6970821Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14101,391,345101,625,639
    nsv6970821RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14101,857,682102,091,976

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18612402duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18612402Submitted genomicNC_000014.9:g.1013
    91345_101625639dup
    GRCh38 (hg38)NC_000014.9Chr14101,391,345101,625,639
    nssv18612402RemappedPerfectNC_000014.8:g.1018
    57682_102091976dup
    GRCh37.p13First PassNC_000014.8Chr14101,857,682102,091,976

    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)
    nssv186124024e-061273858
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