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nsv6866046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:368,317

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1814 SVs from 77 studies. See in: genome view    
    Submitted genomic33,859,162-34,227,478Question Mark
    Overlapping variant regions from other studies: 1821 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):33,859,160-34,227,476Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6866046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr933,859,16234,227,478
    nsv6866046RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr933,859,16034,227,476

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732976duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732976Submitted genomicNC_000009.12:g.338
    59162_34227478dup
    GRCh38 (hg38)NC_000009.12Chr933,859,16234,227,478
    nssv18732976RemappedPerfectNC_000009.11:g.338
    59160_34227476dup
    GRCh37.p13First PassNC_000009.11Chr933,859,16034,227,476

    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)
    nssv187329764e-061274436
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