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nsv6920090

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:304

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 26 studies. See in: genome view    
    Submitted genomic133,035,463-133,035,766Question Mark
    Overlapping variant regions from other studies: 107 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):133,612,049-133,612,352Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6920090Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12133,035,463133,035,766
    nsv6920090RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,612,049133,612,352

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18595600duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18595600Submitted genomicNC_000012.12:g.133
    035463_133035766du
    p
    GRCh38 (hg38)NC_000012.12Chr12133,035,463133,035,766
    nssv18595600RemappedPerfectNC_000012.11:g.133
    612049_133612352du
    p
    GRCh37.p13First PassNC_000012.11Chr12133,612,049133,612,352

    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)
    nssv18595600<0.001138225814
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