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nsv7061383

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:752,193

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4265 SVs from 111 studies. See in: genome view    
    Submitted genomic20,296,571-21,048,763Question Mark
    Overlapping variant regions from other studies: 1829 SVs from 89 studies. See in: genome view    
    Remapped(Score: Pass):20,845,947-21,231,569Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061383Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1920,296,57121,048,763
    nsv7061383RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1920,845,94721,231,569

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759969inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759969Submitted genomicNC_000019.10:g.202
    96571_21048763inv
    GRCh38 (hg38)NC_000019.10Chr1920,296,57121,048,763
    nssv18759969RemappedPassNC_000019.9:g.2084
    5947_21231569inv
    GRCh37.p13First PassNC_000019.9Chr1920,845,94721,231,569

    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)
    nssv187599691.1e-053274078
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