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nsv7073298

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:296,902

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2031 SVs from 100 studies. See in: genome view    
    Submitted genomic40,825,689-41,122,590Question Mark
    Overlapping variant regions from other studies: 2031 SVs from 100 studies. See in: genome view    
    Remapped(Score: Perfect):41,331,594-41,628,495Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073298Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1940,825,68941,122,590
    nsv7073298RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1941,331,59441,628,495

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760732inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760732Submitted genomicNC_000019.10:g.408
    25689_41122590inv
    GRCh38 (hg38)NC_000019.10Chr1940,825,68941,122,590
    nssv18760732RemappedPerfectNC_000019.9:g.4133
    1594_41628495inv
    GRCh37.p13First PassNC_000019.9Chr1941,331,59441,628,495

    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)
    nssv187607326.1e-0516273996
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