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nsv6640478

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,854

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 23 studies. See in: genome view    
    Submitted genomic11,650,734-11,652,587Question Mark
    Overlapping variant regions from other studies: 117 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):11,710,791-11,712,644Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6640478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr111,650,73411,652,587
    nsv6640478RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr111,710,79111,712,644

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18573623duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18573623Submitted genomicNC_000001.11:g.116
    50734_11652587dup
    GRCh38 (hg38)NC_000001.11Chr111,650,73411,652,587
    nssv18573623RemappedPerfectNC_000001.10:g.117
    10791_11712644dup
    GRCh37.p13First PassNC_000001.10Chr111,710,79111,712,644

    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)
    nssv185736234e-061271256
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