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nsv6714556

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

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
    Submitted genomic11,290,797-11,290,930Question Mark
    Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):11,332,483-11,332,616Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6714556Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,290,79711,290,930
    nsv6714556RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,332,48311,332,616

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18668013duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18668013Submitted genomicNC_000003.12:g.112
    90797_11290930dup
    GRCh38 (hg38)NC_000003.12Chr311,290,79711,290,930
    nssv18668013RemappedPerfectNC_000003.11:g.113
    32483_11332616dup
    GRCh37.p13First PassNC_000003.11Chr311,332,48311,332,616

    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)
    nssv18668013<0.00124226646
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