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nsv7073751

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:720,458

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2414 SVs from 112 studies. See in: genome view    
    Submitted genomic49,459,138-50,179,595Question Mark
    Overlapping variant regions from other studies: 2387 SVs from 112 studies. See in: genome view    
    Remapped(Score: Pass):49,480,690-50,138,766Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073751Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1149,459,13850,179,595
    nsv7073751RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1149,480,69050,138,766

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736486inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736486Submitted genomicNC_000011.10:g.494
    59138_50179595inv
    GRCh38 (hg38)NC_000011.10Chr1149,459,13850,179,595
    nssv18736486RemappedPassNC_000011.9:g.4948
    0690_50138766inv
    GRCh37.p13First PassNC_000011.9Chr1149,480,69050,138,766

    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)
    nssv187364861.1e-053274320
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