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nsv6913821

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 15 studies. See in: genome view    
    Submitted genomic113,904,827-113,904,888Question Mark
    Overlapping variant regions from other studies: 84 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):113,775,549-113,775,610Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6913821Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11113,904,827113,904,888
    nsv6913821RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11113,775,549113,775,610

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18587474duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18587474Submitted genomicNC_000011.10:g.113
    904827_113904888du
    p
    GRCh38 (hg38)NC_000011.10Chr11113,904,827113,904,888
    nssv18587474RemappedPerfectNC_000011.9:g.1137
    75549_113775610dup
    GRCh37.p13First PassNC_000011.9Chr11113,775,549113,775,610

    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)
    nssv18587474<0.00158218464
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