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nsv6647227

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,098,532

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 20848 SVs from 132 studies. See in: genome view    
    Submitted genomic20,848,934-27,947,465Question Mark
    Overlapping variant regions from other studies: 20864 SVs from 132 studies. See in: genome view    
    Remapped(Score: Perfect):21,175,427-28,273,976Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6647227Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr120,848,93427,947,465
    nsv6647227RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr121,175,42728,273,976

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18367947deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18367947Submitted genomicNC_000001.11:g.208
    48934_27947465del
    GRCh38 (hg38)NC_000001.11Chr120,848,93427,947,465
    nssv18367947RemappedPerfectNC_000001.10:g.211
    75427_28273976del
    GRCh37.p13First PassNC_000001.10Chr121,175,42728,273,976

    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)
    nssv183679470.04411115251462
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