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nsv6455930

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,165

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 98 SVs from 16 studies. See in: genome view    
    Submitted genomic117,824,778-117,826,942Question Mark
    Overlapping variant regions from other studies: 98 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):117,695,493-117,697,657Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6455930Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11117,824,778117,826,942
    nsv6455930RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11117,695,493117,697,657

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18194972duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18194972Submitted genomicNC_000011.10:g.117
    824778_117826942du
    p
    GRCh38 (hg38)NC_000011.10Chr11117,824,778117,826,942
    nssv18194972RemappedPerfectNC_000011.9:g.1176
    95493_117697657dup
    GRCh37.p13First PassNC_000011.9Chr11117,695,493117,697,657

    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)
    nssv18194972<0.001139284
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