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nsv7051130

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,056,169

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5026 SVs from 104 studies. See in: genome view    
    Submitted genomic196,923,427-197,979,595Question Mark
    Overlapping variant regions from other studies: 5026 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):196,650,298-197,706,466Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051130Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3196,923,427197,979,595
    nsv7051130RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3196,650,298197,706,466

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771454inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771454Submitted genomicNC_000003.12:g.196
    923427_197979595in
    v
    GRCh38 (hg38)NC_000003.12Chr3196,923,427197,979,595
    nssv18771454RemappedPerfectNC_000003.11:g.196
    650298_197706466in
    v
    GRCh37.p13First PassNC_000003.11Chr3196,650,298197,706,466

    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)
    nssv187714541.1e-053274382
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