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nsv6423267

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,498,558

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5418 SVs from 107 studies. See in: genome view    
    Submitted genomic140,419,094-141,917,651Question Mark
    Overlapping variant regions from other studies: 5419 SVs from 107 studies. See in: genome view    
    Remapped(Score: Good):141,429,193-142,999,012Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6423267Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8140,419,094141,917,651
    nsv6423267RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8141,429,193142,999,012

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18231675duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18231675Submitted genomicNC_000008.11:g.140
    419094_141917651du
    p
    GRCh38 (hg38)NC_000008.11Chr8140,419,094141,917,651
    nssv18231675RemappedGoodNC_000008.10:g.141
    429193_142999012du
    p
    GRCh37.p13First PassNC_000008.10Chr8141,429,193142,999,012

    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)
    nssv18231675<0.001233598
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