nsv7070300

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:88,239

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 530 SVs from 88 studies. See in: genome view    
    Submitted genomic113,024,640-113,112,878Question Mark
    Overlapping variant regions from other studies: 530 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):115,786,920-115,875,158Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070300Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9113,024,640113,112,878
    nsv7070300RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9115,786,920115,875,158

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783873inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783873Submitted genomicNC_000009.12:g.113
    024640_113112878in
    v
    GRCh38 (hg38)NC_000009.12Chr9113,024,640113,112,878
    nssv18783873RemappedPerfectNC_000009.11:g.115
    786920_115875158in
    v
    GRCh37.p13First PassNC_000009.11Chr9115,786,920115,875,158

    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)
    nssv187838736.4e-0517275480
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