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nsv6371854

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,926

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 40 studies. See in: genome view    
    Submitted genomic129,115,379-129,149,304Question Mark
    Overlapping variant regions from other studies: 193 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):128,834,222-128,868,147Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6371854Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3129,115,379129,149,304
    nsv6371854RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3128,834,222128,868,147

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18211378duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18211378Submitted genomicNC_000003.12:g.129
    115379_129149304du
    p
    GRCh38 (hg38)NC_000003.12Chr3129,115,379129,149,304
    nssv18211378RemappedPerfectNC_000003.11:g.128
    834222_128868147du
    p
    GRCh37.p13First PassNC_000003.11Chr3128,834,222128,868,147

    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)
    nssv18211378<0.001139256
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