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nsv6780567

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,363

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 177 SVs from 31 studies. See in: genome view    
    Submitted genomic139,264,264-139,309,626Question Mark
    Overlapping variant regions from other studies: 177 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):138,599,953-138,645,315Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6780567Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5139,264,264139,309,626
    nsv6780567RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5138,599,953138,645,315

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18695454duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18695454Submitted genomicNC_000005.10:g.139
    264264_139309626du
    p
    GRCh38 (hg38)NC_000005.10Chr5139,264,264139,309,626
    nssv18695454RemappedPerfectNC_000005.9:g.1385
    99953_138645315dup
    GRCh37.p13First PassNC_000005.9Chr5138,599,953138,645,315

    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)
    nssv186954544e-061275272
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