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nsv6907816

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,086

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 214 SVs from 50 studies. See in: genome view    
    Submitted genomic2,302,022-2,317,107Question Mark
    Overlapping variant regions from other studies: 214 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):2,323,252-2,338,337Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6907816Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr112,302,0222,317,107
    nsv6907816RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr112,323,2522,338,337

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18345568deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18345568Submitted genomicNC_000011.10:g.230
    2022_2317107del
    GRCh38 (hg38)NC_000011.10Chr112,302,0222,317,107
    nssv18345568RemappedPerfectNC_000011.9:g.2323
    252_2338337del
    GRCh37.p13First PassNC_000011.9Chr112,323,2522,338,337

    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)
    nssv183455681.1e-053276176
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