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nsv7022394

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 283 SVs from 64 studies. See in: genome view    
    Submitted genomic43,136,788-43,164,687Question Mark
    Overlapping variant regions from other studies: 283 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):43,532,794-43,560,693Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7022394Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2243,136,78843,164,687
    nsv7022394RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2243,532,79443,560,693

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18652252duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18652252Submitted genomicNC_000022.11:g.431
    36788_43164687dup
    GRCh38 (hg38)NC_000022.11Chr2243,136,78843,164,687
    nssv18652252RemappedPerfectNC_000022.10:g.435
    32794_43560693dup
    GRCh37.p13First PassNC_000022.10Chr2243,532,79443,560,693

    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)
    nssv186522524e-061275224
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