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nsv7069372

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,631

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 394 SVs from 77 studies. See in: genome view    
    Submitted genomic112,994,393-113,060,023Question Mark
    Overlapping variant regions from other studies: 394 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):115,756,673-115,822,303Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069372Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9112,994,393113,060,023
    nsv7069372RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9115,756,673115,822,303

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783870inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783870Submitted genomicNC_000009.12:g.112
    994393_113060023in
    v
    GRCh38 (hg38)NC_000009.12Chr9112,994,393113,060,023
    nssv18783870RemappedPerfectNC_000009.11:g.115
    756673_115822303in
    v
    GRCh37.p13First PassNC_000009.11Chr9115,756,673115,822,303

    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)
    nssv187838701.1e-053273428
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