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nsv6718881

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,840,425

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 19062 SVs from 122 studies. See in: genome view    
    Submitted genomic3,908,216-9,748,640Question Mark
    Overlapping variant regions from other studies: 19075 SVs from 122 studies. See in: genome view    
    Remapped(Score: Good):3,909,943-9,750,264Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6718881Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr43,908,2169,748,640
    nsv6718881RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr43,909,9439,750,264

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18497491deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18497491Submitted genomicNC_000004.12:g.390
    8216_9748640del
    GRCh38 (hg38)NC_000004.12Chr43,908,2169,748,640
    nssv18497491RemappedGoodNC_000004.11:g.390
    9943_9750264del
    GRCh37.p13First PassNC_000004.11Chr43,909,9439,750,264

    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)
    nssv184974914e-061276086
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