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nsv6408594

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:320,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 959 SVs from 80 studies. See in: genome view    
    Submitted genomic140,515,601-140,836,000Question Mark
    Overlapping variant regions from other studies: 624 SVs from 63 studies. See in: genome view    
    Remapped(Score: Pass):139,895,186-140,144,409Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6408594Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5140,515,601140,836,000
    nsv6408594RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5139,895,186140,144,409

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18215084duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18215084Submitted genomicNC_000005.10:g.140
    515601_140836000du
    p
    GRCh38 (hg38)NC_000005.10Chr5140,515,601140,836,000
    nssv18215084RemappedPassNC_000005.9:g.1398
    95186_140144409dup
    GRCh37.p13First PassNC_000005.9Chr5139,895,186140,144,409

    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)
    nssv18215084<0.001138648
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