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nsv6912121

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:90,742

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 266 SVs from 42 studies. See in: genome view    
    Submitted genomic117,857,085-117,947,826Question Mark
    Overlapping variant regions from other studies: 266 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):117,727,800-117,818,541Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912121Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11117,857,085117,947,826
    nsv6912121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11117,727,800117,818,541

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18582550duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18582550Submitted genomicNC_000011.10:g.117
    857085_117947826du
    p
    GRCh38 (hg38)NC_000011.10Chr11117,857,085117,947,826
    nssv18582550RemappedPerfectNC_000011.9:g.1177
    27800_117818541dup
    GRCh37.p13First PassNC_000011.9Chr11117,727,800117,818,541

    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)
    nssv185825503.6e-0510274140
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