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nsv6492169

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:114,615

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 703 SVs from 71 studies. See in: genome view    
    Submitted genomic132,837,112-132,951,726Question Mark
    Overlapping variant regions from other studies: 703 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):133,413,698-133,528,312Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6492169Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12132,837,112132,951,726
    nsv6492169RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,413,698133,528,312

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18185289duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18185289Submitted genomicNC_000012.12:g.132
    837112_132951726du
    p
    GRCh38 (hg38)NC_000012.12Chr12132,837,112132,951,726
    nssv18185289RemappedPerfectNC_000012.11:g.133
    413698_133528312du
    p
    GRCh37.p13First PassNC_000012.11Chr12133,413,698133,528,312

    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)
    nssv18185289<0.001139208
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