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nsv6474741

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 222 SVs from 46 studies. See in: genome view    
    Submitted genomic112,201,101-112,236,800Question Mark
    Overlapping variant regions from other studies: 222 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):112,071,824-112,107,523Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6474741Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11112,201,101112,236,800
    nsv6474741RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11112,071,824112,107,523

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18179106duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18179106Submitted genomicNC_000011.10:g.112
    201101_112236800du
    p
    GRCh38 (hg38)NC_000011.10Chr11112,201,101112,236,800
    nssv18179106RemappedPerfectNC_000011.9:g.1120
    71824_112107523dup
    GRCh37.p13First PassNC_000011.9Chr11112,071,824112,107,523

    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)
    nssv18179106<0.0012539242
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