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nsv6338031

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,932

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 19 studies. See in: genome view    
    Submitted genomic222,424,612-222,429,543Question Mark
    Overlapping variant regions from other studies: 107 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):223,289,331-223,294,262Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6338031Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2222,424,612222,429,543
    nsv6338031RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2223,289,331223,294,262

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18206257duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18206257Submitted genomicNC_000002.12:g.222
    424612_222429543du
    p
    GRCh38 (hg38)NC_000002.12Chr2222,424,612222,429,543
    nssv18206257RemappedPerfectNC_000002.11:g.223
    289331_223294262du
    p
    GRCh37.p13First PassNC_000002.11Chr2223,289,331223,294,262

    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)
    nssv18206257<0.001139262
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