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nsv6649169

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,806

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 22 studies. See in: genome view    
    Submitted genomic34,005,918-34,008,723Question Mark
    Overlapping variant regions from other studies: 92 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):34,471,519-34,474,324Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6649169Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr134,005,91834,008,723
    nsv6649169RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr134,471,51934,474,324

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18610528duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18610528Submitted genomicNC_000001.11:g.340
    05918_34008723dup
    GRCh38 (hg38)NC_000001.11Chr134,005,91834,008,723
    nssv18610528RemappedPerfectNC_000001.10:g.344
    71519_34474324dup
    GRCh37.p13First PassNC_000001.10Chr134,471,51934,474,324

    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)
    nssv186105285.7e-0516272402
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