nsv7072924

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,763,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8282 SVs from 131 studies. See in: genome view    
    Submitted genomic23,614,290-25,377,289Question Mark
    Overlapping variant regions from other studies: 9168 SVs from 133 studies. See in: genome view    
    Remapped(Score: Good):23,956,477-25,773,256Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072924Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2223,614,29025,377,289
    nsv7072924RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2223,956,47725,773,256

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763843inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763843Submitted genomicNC_000022.11:g.236
    14290_25377289inv
    GRCh38 (hg38)NC_000022.11Chr2223,614,29025,377,289
    nssv18763843RemappedGoodNC_000022.10:g.239
    56477_25773256inv
    GRCh37.p13First PassNC_000022.10Chr2223,956,47725,773,256

    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)
    nssv187638431.1e-053272614
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