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nsv7075196

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,062,821

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 24482 SVs from 129 studies. See in: genome view    
    Submitted genomic130,990,409-137,053,229Question Mark
    Overlapping variant regions from other studies: 24281 SVs from 129 studies. See in: genome view    
    Remapped(Score: Good):133,865,796-139,947,681Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075196Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9130,990,409137,053,229
    nsv7075196RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9133,865,796139,947,681

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785507inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785507Submitted genomicNC_000009.12:g.130
    990409_137053229in
    v
    GRCh38 (hg38)NC_000009.12Chr9130,990,409137,053,229
    nssv18785507RemappedGoodNC_000009.11:g.133
    865796_139947681in
    v
    GRCh37.p13First PassNC_000009.11Chr9133,865,796139,947,681

    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)
    nssv187855077e-062276264
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