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nsv6786405

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,174

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 80 SVs from 14 studies. See in: genome view    
    Submitted genomic132,219,309-132,223,482Question Mark
    Overlapping variant regions from other studies: 80 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):131,555,002-131,559,175Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6786405Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5132,219,309132,223,482
    nsv6786405RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5131,555,002131,559,175

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18694789duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18694789Submitted genomicNC_000005.10:g.132
    219309_132223482du
    p
    GRCh38 (hg38)NC_000005.10Chr5132,219,309132,223,482
    nssv18694789RemappedPerfectNC_000005.9:g.1315
    55002_131559175dup
    GRCh37.p13First PassNC_000005.9Chr5131,555,002131,559,175

    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)
    nssv186947892.1e-056274352
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