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nsv7043408

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,420,435

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4613 SVs from 112 studies. See in: genome view    
    Submitted genomic131,584,332-133,004,766Question Mark
    Overlapping variant regions from other studies: 4742 SVs from 112 studies. See in: genome view    
    Remapped(Score: Perfect):132,341,905-133,762,339Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043408Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2131,584,332133,004,766
    nsv7043408RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2132,341,905133,762,339

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767629inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767629Submitted genomicNC_000002.12:g.131
    584332_133004766in
    v
    GRCh38 (hg38)NC_000002.12Chr2131,584,332133,004,766
    nssv18767629RemappedPerfectNC_000002.11:g.132
    341905_133762339in
    v
    GRCh37.p13First PassNC_000002.11Chr2132,341,905133,762,339

    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)
    nssv187676292.9e-058274724
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