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nsv6991827

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:193

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 81 SVs from 17 studies. See in: genome view    
    Submitted genomic27,948,683-27,948,875Question Mark
    Overlapping variant regions from other studies: 81 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):26,275,709-26,275,901Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6991827Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1727,948,68327,948,875
    nsv6991827RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1726,275,70926,275,901

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626091duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626091Submitted genomicNC_000017.11:g.279
    48683_27948875dup
    GRCh38 (hg38)NC_000017.11Chr1727,948,68327,948,875
    nssv18626091RemappedPerfectNC_000017.10:g.262
    75709_26275901dup
    GRCh37.p13First PassNC_000017.10Chr1726,275,70926,275,901

    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)
    nssv18626091<0.00132232326
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