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nsv6986977

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,782

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 252 SVs from 38 studies. See in: genome view    
    Submitted genomic74,608,737-74,622,518Question Mark
    Overlapping variant regions from other studies: 252 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):72,604,876-72,618,657Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6986977Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1774,608,73774,622,518
    nsv6986977RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1772,604,87672,618,657

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18415141deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18415141Submitted genomicNC_000017.11:g.746
    08737_74622518del
    GRCh38 (hg38)NC_000017.11Chr1774,608,73774,622,518
    nssv18415141RemappedPerfectNC_000017.10:g.726
    04876_72618657del
    GRCh37.p13First PassNC_000017.10Chr1772,604,87672,618,657

    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)
    nssv184151414e-061276212
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