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nsv6980247

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:843,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2604 SVs from 95 studies. See in: genome view    
    Submitted genomic36,753,135-37,596,834Question Mark
    Overlapping variant regions from other studies: 2308 SVs from 93 studies. See in: genome view    
    Remapped(Score: Pass):35,168,060-35,888,667Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6980247Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1736,753,13537,596,834
    nsv6980247RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1735,168,06035,888,667

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628608duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628608Submitted genomicNC_000017.11:g.367
    53135_37596834dup
    GRCh38 (hg38)NC_000017.11Chr1736,753,13537,596,834
    nssv18628608RemappedPassNC_000017.10:g.351
    68060_35888667dup
    GRCh37.p13First PassNC_000017.10Chr1735,168,06035,888,667

    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)
    nssv186286084e-061276006
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