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nsv7051798

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:164,508

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 448 SVs from 56 studies. See in: genome view    
    Submitted genomic133,461,213-133,625,720Question Mark
    Overlapping variant regions from other studies: 448 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):134,218,784-134,383,291Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051798Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2133,461,213133,625,720
    nsv7051798RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2134,218,784134,383,291

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765742inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765742Submitted genomicNC_000002.12:g.133
    461213_133625720in
    v
    GRCh38 (hg38)NC_000002.12Chr2133,461,213133,625,720
    nssv18765742RemappedPerfectNC_000002.11:g.134
    218784_134383291in
    v
    GRCh37.p13First PassNC_000002.11Chr2134,218,784134,383,291

    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)
    nssv18765742<0.001108273394
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