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nsv6875887

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:91,347

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 571 SVs from 67 studies. See in: genome view    
    Submitted genomic142,258,235-142,349,581Question Mark
    Overlapping variant regions from other studies: 571 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):143,339,596-143,430,942Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875887Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8142,258,235142,349,581
    nsv6875887RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8143,339,596143,430,942

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18750814duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18750814Submitted genomicNC_000008.11:g.142
    258235_142349581du
    p
    GRCh38 (hg38)NC_000008.11Chr8142,258,235142,349,581
    nssv18750814RemappedPerfectNC_000008.10:g.143
    339596_143430942du
    p
    GRCh37.p13First PassNC_000008.10Chr8143,339,596143,430,942

    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)
    nssv187508144e-061275090
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