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nsv6648783

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:524,036

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2703 SVs from 95 studies. See in: genome view    
    Submitted genomic3,557,253-4,081,288Question Mark
    Overlapping variant regions from other studies: 2701 SVs from 95 studies. See in: genome view    
    Remapped(Score: Pass):3,473,817-4,141,348Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6648783Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr13,557,2534,081,288
    nsv6648783RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr13,473,8174,141,348

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18610699duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18610699Submitted genomicNC_000001.11:g.355
    7253_4081288dup
    GRCh38 (hg38)NC_000001.11Chr13,557,2534,081,288
    nssv18610699RemappedPassNC_000001.10:g.347
    3817_4141348dup
    GRCh37.p13First PassNC_000001.10Chr13,473,8174,141,348

    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)
    nssv186106994e-061274796
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