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nsv6744410

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,586

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 181 SVs from 41 studies. See in: genome view    
    Submitted genomic141,692,156-141,721,741Question Mark
    Overlapping variant regions from other studies: 181 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):142,613,309-142,642,894Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6744410Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4141,692,156141,721,741
    nsv6744410RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4142,613,309142,642,894

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18685224duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18685224Submitted genomicNC_000004.12:g.141
    692156_141721741du
    p
    GRCh38 (hg38)NC_000004.12Chr4141,692,156141,721,741
    nssv18685224RemappedPerfectNC_000004.11:g.142
    613309_142642894du
    p
    GRCh37.p13First PassNC_000004.11Chr4142,613,309142,642,894

    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)
    nssv186852244e-061273978
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