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nsv6841173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 163 SVs from 12 studies. See in: genome view    
    Submitted genomic23,851,171-23,851,335Question Mark
    Overlapping variant regions from other studies: 163 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):23,708,684-23,708,848Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6841173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr823,851,17123,851,335
    nsv6841173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr823,708,68423,708,848

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731759duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731759Submitted genomicNC_000008.11:g.238
    51171_23851335dup
    GRCh38 (hg38)NC_000008.11Chr823,851,17123,851,335
    nssv18731759RemappedPerfectNC_000008.10:g.237
    08684_23708848dup
    GRCh37.p13First PassNC_000008.10Chr823,708,68423,708,848

    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)
    nssv187317596.9e-0515228120
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