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nsv6723679

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:294

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 19 studies. See in: genome view    
    Submitted genomic141,109,347-141,109,640Question Mark
    Overlapping variant regions from other studies: 103 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):140,828,189-140,828,482Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6723679Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3141,109,347141,109,640
    nsv6723679RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3140,828,189140,828,482

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18673043duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18673043Submitted genomicNC_000003.12:g.141
    109347_141109640du
    p
    GRCh38 (hg38)NC_000003.12Chr3141,109,347141,109,640
    nssv18673043RemappedPerfectNC_000003.11:g.140
    828189_140828482du
    p
    GRCh37.p13First PassNC_000003.11Chr3140,828,189140,828,482

    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)
    nssv18673043<0.0015217098
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