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nsv6908160

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view    
    Submitted genomic110,433,209-110,435,608Question Mark
    Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):110,303,933-110,306,332Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6908160Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11110,433,209110,435,608
    nsv6908160RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11110,303,933110,306,332

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18342754deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18342754Submitted genomicNC_000011.10:g.110
    433209_110435608de
    l
    GRCh38 (hg38)NC_000011.10Chr11110,433,209110,435,608
    nssv18342754RemappedPerfectNC_000011.9:g.1103
    03933_110306332del
    GRCh37.p13First PassNC_000011.9Chr11110,303,933110,306,332

    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)
    nssv183427541.1e-053275566
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