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nsv6351471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,099

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 266 SVs from 43 studies. See in: genome view    
    Submitted genomic237,836,898-237,866,996Question Mark
    Overlapping variant regions from other studies: 266 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):238,745,541-238,775,639Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6351471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2237,836,898237,866,996
    nsv6351471RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2238,745,541238,775,639

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18208364duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18208364Submitted genomicNC_000002.12:g.237
    836898_237866996du
    p
    GRCh38 (hg38)NC_000002.12Chr2237,836,898237,866,996
    nssv18208364RemappedPerfectNC_000002.11:g.238
    745541_238775639du
    p
    GRCh37.p13First PassNC_000002.11Chr2238,745,541238,775,639

    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)
    nssv18208364<0.001639266
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