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nsv7076436

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85,825

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1555 SVs from 88 studies. See in: genome view    
    Submitted genomic22,495,892-22,581,716Question Mark
    Overlapping variant regions from other studies: 1566 SVs from 88 studies. See in: genome view    
    Remapped(Score: Pass):22,850,211-22,924,180Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076436Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2222,495,89222,581,716
    nsv7076436RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2222,850,21122,924,180

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763815inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763815Submitted genomicNC_000022.11:g.224
    95892_22581716inv
    GRCh38 (hg38)NC_000022.11Chr2222,495,89222,581,716
    nssv18763815RemappedPassNC_000022.10:g.228
    50211_22924180inv
    GRCh37.p13First PassNC_000022.10Chr2222,850,21122,924,180

    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)
    nssv187638157e-062276258
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