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nsv6795442

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,221,096

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2342 SVs from 83 studies. See in: genome view    
    Submitted genomic39,085,006-40,306,101Question Mark
    Overlapping variant regions from other studies: 2340 SVs from 83 studies. See in: genome view    
    Remapped(Score: Good):39,052,782-40,273,840Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6795442Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr639,085,00640,306,101
    nsv6795442RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr639,052,78240,273,840

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715650duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715650Submitted genomicNC_000006.12:g.390
    85006_40306101dup
    GRCh38 (hg38)NC_000006.12Chr639,085,00640,306,101
    nssv18715650RemappedGoodNC_000006.11:g.390
    52782_40273840dup
    GRCh37.p13First PassNC_000006.11Chr639,052,78240,273,840

    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)
    nssv187156504e-061275990
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