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nsv6991508

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,051,440

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4202 SVs from 103 studies. See in: genome view    
    Submitted genomic42,821,629-43,873,068Question Mark
    Overlapping variant regions from other studies: 4014 SVs from 102 studies. See in: genome view    
    Remapped(Score: Pass):40,973,647-41,950,436Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6991508Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1742,821,62943,873,068
    nsv6991508RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1740,973,64741,950,436

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626917duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626917Submitted genomicNC_000017.11:g.428
    21629_43873068dup
    GRCh38 (hg38)NC_000017.11Chr1742,821,62943,873,068
    nssv18626917RemappedPassNC_000017.10:g.409
    73647_41950436dup
    GRCh37.p13First PassNC_000017.10Chr1740,973,64741,950,436

    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)
    nssv186269174e-061275506
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