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nsv6884507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:390,546

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1942 SVs from 92 studies. See in: genome view    
    Submitted genomic135,999,993-136,390,538Question Mark
    Overlapping variant regions from other studies: 1867 SVs from 92 studies. See in: genome view    
    Remapped(Score: Good):138,891,839-139,284,990Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6884507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9135,999,993136,390,538
    nsv6884507RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9138,891,839139,284,990

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18746400duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18746400Submitted genomicNC_000009.12:g.135
    999993_136390538du
    p
    GRCh38 (hg38)NC_000009.12Chr9135,999,993136,390,538
    nssv18746400RemappedGoodNC_000009.11:g.138
    891839_139284990du
    p
    GRCh37.p13First PassNC_000009.11Chr9138,891,839139,284,990

    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)
    nssv187464002.7e-054147486
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