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nsv6778130

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:569

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 17 studies. See in: genome view    
    Submitted genomic141,485,723-141,486,291Question Mark
    Overlapping variant regions from other studies: 83 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):140,865,290-140,865,858Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6778130Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5141,485,723141,486,291
    nsv6778130RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,865,290140,865,858

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18699152duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18699152Submitted genomicNC_000005.10:g.141
    485723_141486291du
    p
    GRCh38 (hg38)NC_000005.10Chr5141,485,723141,486,291
    nssv18699152RemappedPerfectNC_000005.9:g.1408
    65290_140865858dup
    GRCh37.p13First PassNC_000005.9Chr5140,865,290140,865,858

    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)
    nssv186991524.3e-0511249264
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