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nsv6795271

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:692,645

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1594 SVs from 80 studies. See in: genome view    
    Submitted genomic49,332,174-50,024,818Question Mark
    Overlapping variant regions from other studies: 1594 SVs from 80 studies. See in: genome view    
    Remapped(Score: Good):49,299,844-49,992,531Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6795271Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr649,332,17450,024,818
    nsv6795271RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr649,299,84449,992,531

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18715884duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18715884Submitted genomicNC_000006.12:g.493
    32174_50024818dup
    GRCh38 (hg38)NC_000006.12Chr649,332,17450,024,818
    nssv18715884RemappedGoodNC_000006.11:g.492
    99844_49992531dup
    GRCh37.p13First PassNC_000006.11Chr649,299,84449,992,531

    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)
    nssv187158844e-061275034
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