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nsv6668670

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,407

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 26 studies. See in: genome view    
    Submitted genomic3,412,661-3,416,067Question Mark
    Overlapping variant regions from other studies: 128 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):3,416,432-3,419,838Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6668670Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr23,412,6613,416,067
    nsv6668670RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr23,416,4323,419,838

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18464192deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18464192Submitted genomicNC_000002.12:g.341
    2661_3416067del
    GRCh38 (hg38)NC_000002.12Chr23,412,6613,416,067
    nssv18464192RemappedPerfectNC_000002.11:g.341
    6432_3419838del
    GRCh37.p13First PassNC_000002.11Chr23,416,4323,419,838

    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)
    nssv184641921.8e-055276268
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