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nsv6699636

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64,140

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 398 SVs from 55 studies. See in: genome view    
    Submitted genomic238,880,031-238,944,170Question Mark
    Overlapping variant regions from other studies: 346 SVs from 55 studies. See in: genome view    
    Remapped(Score: Pass):239,788,672-239,865,866Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6699636Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2238,880,031238,944,170
    nsv6699636RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2239,788,672239,865,866

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18663857duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18663857Submitted genomicNC_000002.12:g.238
    880031_238944170du
    p
    GRCh38 (hg38)NC_000002.12Chr2238,880,031238,944,170
    nssv18663857RemappedPassNC_000002.11:g.239
    788672_239865866du
    p
    GRCh37.p13First PassNC_000002.11Chr2239,788,672239,865,866

    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)
    nssv186638572.8e-058274906
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