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nsv6875611

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:545

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 189 SVs from 45 studies. See in: genome view    
    Submitted genomic142,272,145-142,272,689Question Mark
    Overlapping variant regions from other studies: 189 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):143,353,506-143,354,050Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875611Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8142,272,145142,272,689
    nsv6875611RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8143,353,506143,354,050

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18735332duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18735332Submitted genomicNC_000008.11:g.142
    272145_142272689du
    p
    GRCh38 (hg38)NC_000008.11Chr8142,272,145142,272,689
    nssv18735332RemappedPerfectNC_000008.10:g.143
    353506_143354050du
    p
    GRCh37.p13First PassNC_000008.10Chr8143,353,506143,354,050

    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)
    nssv187353320.26538520147006
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