nsv7058764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:955

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 76 SVs from 23 studies. See in: genome view    
    Submitted genomic124,259,061-124,260,015Question Mark
    Overlapping variant regions from other studies: 76 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):127,021,340-127,022,294Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058764Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9124,259,061124,260,015
    nsv7058764RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9127,021,340127,022,294

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784354inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784354Submitted genomicNC_000009.12:g.124
    259061_124260015in
    v
    GRCh38 (hg38)NC_000009.12Chr9124,259,061124,260,015
    nssv18784354RemappedPerfectNC_000009.11:g.127
    021340_127022294in
    v
    GRCh37.p13First PassNC_000009.11Chr9127,021,340127,022,294

    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)
    nssv187843541.1e-053276262
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