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nsv6663744

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:440,274

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1167 SVs from 88 studies. See in: genome view    
    Submitted genomic228,275,386-228,715,659Question Mark
    Overlapping variant regions from other studies: 1169 SVs from 88 studies. See in: genome view    
    Remapped(Score: Pass):228,463,087-228,851,406Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6663744Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1228,275,386228,715,659
    nsv6663744RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1228,463,087228,851,406

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609412duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609412Submitted genomicNC_000001.11:g.228
    275386_228715659du
    p
    GRCh38 (hg38)NC_000001.11Chr1228,275,386228,715,659
    nssv18609412RemappedPassNC_000001.10:g.228
    463087_228851406du
    p
    GRCh37.p13First PassNC_000001.10Chr1228,463,087228,851,406

    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)
    nssv186094122.5e-057273750
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