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nsv6734556

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 24 studies. See in: genome view    
    Submitted genomic179,615,001-179,629,500Question Mark
    Overlapping variant regions from other studies: 110 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):179,332,789-179,347,288Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6734556Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3179,615,001179,629,500
    nsv6734556RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3179,332,789179,347,288

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18674373duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18674373Submitted genomicNC_000003.12:g.179
    615001_179629500du
    p
    GRCh38 (hg38)NC_000003.12Chr3179,615,001179,629,500
    nssv18674373RemappedPerfectNC_000003.11:g.179
    332789_179347288du
    p
    GRCh37.p13First PassNC_000003.11Chr3179,332,789179,347,288

    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)
    nssv186743735.7e-0516272498
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