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nsv7049846

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 20 studies. See in: genome view    
    Submitted genomic122,823,462-122,823,490Question Mark
    Overlapping variant regions from other studies: 104 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):122,542,309-122,542,337Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7049846Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3122,823,462122,823,490
    nsv7049846RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3122,542,309122,542,337

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769360inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769360Submitted genomicNC_000003.12:g.122
    823462_122823490in
    v
    GRCh38 (hg38)NC_000003.12Chr3122,823,462122,823,490
    nssv18769360RemappedPerfectNC_000003.11:g.122
    542309_122542337in
    v
    GRCh37.p13First PassNC_000003.11Chr3122,542,309122,542,337

    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)
    nssv18769360<0.001129274608
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