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nsv6899735

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,176

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 34 studies. See in: genome view    
    Submitted genomic68,106,163-68,111,338Question Mark
    Overlapping variant regions from other studies: 97 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):67,873,630-67,878,805Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6899735Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1168,106,16368,111,338
    nsv6899735RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,873,63067,878,805

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351387deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351387Submitted genomicNC_000011.10:g.681
    06163_68111338del
    GRCh38 (hg38)NC_000011.10Chr1168,106,16368,111,338
    nssv18351387RemappedPerfectNC_000011.9:g.6787
    3630_67878805del
    GRCh37.p13First PassNC_000011.9Chr1167,873,63067,878,805

    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)
    nssv183513871.4e-054276038
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