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nsv7037586

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:168,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 492 SVs from 58 studies. See in: genome view    
    Submitted genomic34,581,801-34,750,500Question Mark
    Overlapping variant regions from other studies: 495 SVs from 58 studies. See in: genome view    
    Remapped(Score: Good):35,954,099-36,122,797Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7037586Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2134,581,80134,750,500
    nsv7037586RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2135,954,09936,122,797

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18647262duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18647262Submitted genomicNC_000021.9:g.3458
    1801_34750500dup
    GRCh38 (hg38)NC_000021.9Chr2134,581,80134,750,500
    nssv18647262RemappedGoodNC_000021.8:g.3595
    4099_36122797dup
    GRCh37.p13First PassNC_000021.8Chr2135,954,09936,122,797

    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)
    nssv186472621.1e-053275980
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