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nsv6842117

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:196

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 18 studies. See in: genome view    
    Submitted genomic89,934,358-89,934,553Question Mark
    Overlapping variant regions from other studies: 142 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):90,946,586-90,946,781Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6842117Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr889,934,35889,934,553
    nsv6842117RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr890,946,58690,946,781

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18742728duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18742728Submitted genomicNC_000008.11:g.899
    34358_89934553dup
    GRCh38 (hg38)NC_000008.11Chr889,934,35889,934,553
    nssv18742728RemappedPerfectNC_000008.10:g.909
    46586_90946781dup
    GRCh37.p13First PassNC_000008.10Chr890,946,58690,946,781

    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)
    nssv187427284e-061233832
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