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nsv7074930

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:657,291

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2585 SVs from 98 studies. See in: genome view    
    Submitted genomic63,711,150-64,368,440Question Mark
    Overlapping variant regions from other studies: 2585 SVs from 98 studies. See in: genome view    
    Remapped(Score: Perfect):64,285,283-64,942,572Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074930Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1363,711,15064,368,440
    nsv7074930RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1364,285,28364,942,572

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753698inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753698Submitted genomicNC_000013.11:g.637
    11150_64368440inv
    GRCh38 (hg38)NC_000013.11Chr1363,711,15064,368,440
    nssv18753698RemappedPerfectNC_000013.10:g.642
    85283_64942572inv
    GRCh37.p13First PassNC_000013.10Chr1364,285,28364,942,572

    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)
    nssv18753698<0.00128272474
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