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nsv6914046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:40,093

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 314 SVs from 49 studies. See in: genome view    
    Submitted genomic124,203,265-124,243,357Question Mark
    Overlapping variant regions from other studies: 328 SVs from 52 studies. See in: genome view    
    Remapped(Score: Good):124,073,972-124,114,105Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6914046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11124,203,265124,243,357
    nsv6914046RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11124,073,972124,114,105

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18343907deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18343907Submitted genomicNC_000011.10:g.124
    203265_124243357de
    l
    GRCh38 (hg38)NC_000011.10Chr11124,203,265124,243,357
    nssv18343907RemappedGoodNC_000011.9:g.1240
    73972_124114105del
    GRCh37.p13First PassNC_000011.9Chr11124,073,972124,114,105

    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)
    nssv183439074e-061276202
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