nsv7048316

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,379,449

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10481 SVs from 110 studies. See in: genome view    
    Submitted genomic217,690,925-222,070,373Question Mark
    Overlapping variant regions from other studies: 10481 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):218,555,648-222,935,092Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048316Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2217,690,925222,070,373
    nsv7048316RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2218,555,648222,935,092

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767407inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767407Submitted genomicNC_000002.12:g.217
    690925_222070373in
    v
    GRCh38 (hg38)NC_000002.12Chr2217,690,925222,070,373
    nssv18767407RemappedPerfectNC_000002.11:g.218
    555648_222935092in
    v
    GRCh37.p13First PassNC_000002.11Chr2218,555,648222,935,092

    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)
    nssv187674074e-061276268
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