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nsv7052794

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:87,359

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 299 SVs from 61 studies. See in: genome view    
    Submitted genomic133,626,700-133,714,058Question Mark
    Overlapping variant regions from other studies: 299 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):134,384,271-134,471,629Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052794Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2133,626,700133,714,058
    nsv7052794RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2134,384,271134,471,629

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765747inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765747Submitted genomicNC_000002.12:g.133
    626700_133714058in
    v
    GRCh38 (hg38)NC_000002.12Chr2133,626,700133,714,058
    nssv18765747RemappedPerfectNC_000002.11:g.134
    384271_134471629in
    v
    GRCh37.p13First PassNC_000002.11Chr2134,384,271134,471,629

    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)
    nssv187657474e-060276268
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