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nsv6540095

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,134,477

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 13662 SVs from 140 studies. See in: genome view    
    Submitted genomic20,268,331-23,402,807Question Mark
    Overlapping variant regions from other studies: 14826 SVs from 140 studies. See in: genome view    
    Remapped(Score: Pass):20,255,854-23,744,994Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6540095Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2220,268,33123,402,807
    nsv6540095RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2220,255,85423,744,994

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18204558duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18204558Submitted genomicNC_000022.11:g.202
    68331_23402807dup
    GRCh38 (hg38)NC_000022.11Chr2220,268,33123,402,807
    nssv18204558RemappedPassNC_000022.10:g.202
    55854_23744994dup
    GRCh37.p13First PassNC_000022.10Chr2220,255,85423,744,994

    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)
    nssv18204558<0.001138788
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