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nsv6780292

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:77,280

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 263 SVs from 40 studies. See in: genome view    
    Submitted genomic132,866,422-132,943,701Question Mark
    Overlapping variant regions from other studies: 263 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):132,202,114-132,279,393Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6780292Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5132,866,422132,943,701
    nsv6780292RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5132,202,114132,279,393

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18698480duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18698480Submitted genomicNC_000005.10:g.132
    866422_132943701du
    p
    GRCh38 (hg38)NC_000005.10Chr5132,866,422132,943,701
    nssv18698480RemappedPerfectNC_000005.9:g.1322
    02114_132279393dup
    GRCh37.p13First PassNC_000005.9Chr5132,202,114132,279,393

    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)
    nssv186984804e-061275840
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