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nsv6875011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69,770

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 346 SVs from 66 studies. See in: genome view    
    Submitted genomic112,968,210-113,037,979Question Mark
    Overlapping variant regions from other studies: 346 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):115,730,490-115,800,259Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9112,968,210113,037,979
    nsv6875011RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9115,730,490115,800,259

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749993duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749993Submitted genomicNC_000009.12:g.112
    968210_113037979du
    p
    GRCh38 (hg38)NC_000009.12Chr9112,968,210113,037,979
    nssv18749993RemappedPerfectNC_000009.11:g.115
    730490_115800259du
    p
    GRCh37.p13First PassNC_000009.11Chr9115,730,490115,800,259

    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)
    nssv187499932.1e-056273388
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