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nsv7061375

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:625,449

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2229 SVs from 84 studies. See in: genome view    
    Submitted genomic111,842,382-112,467,830Question Mark
    Overlapping variant regions from other studies: 2229 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):114,604,662-115,230,110Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061375Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9111,842,382112,467,830
    nsv7061375RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9114,604,662115,230,110

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783853inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783853Submitted genomicNC_000009.12:g.111
    842382_112467830in
    v
    GRCh38 (hg38)NC_000009.12Chr9111,842,382112,467,830
    nssv18783853RemappedPerfectNC_000009.11:g.114
    604662_115230110in
    v
    GRCh37.p13First PassNC_000009.11Chr9114,604,662115,230,110

    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)
    nssv187838534e-061276268
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