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nsv6459453

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:40,201

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 349 SVs from 51 studies. See in: genome view    
    Submitted genomic124,225,572-124,265,772Question Mark
    Overlapping variant regions from other studies: 350 SVs from 49 studies. See in: genome view    
    Remapped(Score: Good):124,096,277-124,135,668Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6459453Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11124,225,572124,265,772
    nsv6459453RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11124,096,277124,135,668

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18180097duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18180097Submitted genomicNC_000011.10:g.124
    225572_124265772du
    p
    GRCh38 (hg38)NC_000011.10Chr11124,225,572124,265,772
    nssv18180097RemappedGoodNC_000011.9:g.1240
    96277_124135668dup
    GRCh37.p13First PassNC_000011.9Chr11124,096,277124,135,668

    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)
    nssv18180097<0.001138992
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