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nsv6839344

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:154,065

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 493 SVs from 50 studies. See in: genome view    
    Submitted genomic116,890,235-117,044,299Question Mark
    Overlapping variant regions from other studies: 493 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):117,902,474-118,056,538Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6839344Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8116,890,235117,044,299
    nsv6839344RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8117,902,474118,056,538

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18730934duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18730934Submitted genomicNC_000008.11:g.116
    890235_117044299du
    p
    GRCh38 (hg38)NC_000008.11Chr8116,890,235117,044,299
    nssv18730934RemappedPerfectNC_000008.10:g.117
    902474_118056538du
    p
    GRCh37.p13First PassNC_000008.10Chr8117,902,474118,056,538

    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)
    nssv187309344e-061275916
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