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nsv7074978

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,651,208

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3791 SVs from 90 studies. See in: genome view    
    Submitted genomic106,755,903-108,407,110Question Mark
    Overlapping variant regions from other studies: 3791 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):109,518,184-111,169,390Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074978Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9106,755,903108,407,110
    nsv7074978RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9109,518,184111,169,390

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783181inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783181Submitted genomicNC_000009.12:g.106
    755903_108407110in
    v
    GRCh38 (hg38)NC_000009.12Chr9106,755,903108,407,110
    nssv18783181RemappedPerfectNC_000009.11:g.109
    518184_111169390in
    v
    GRCh37.p13First PassNC_000009.11Chr9109,518,184111,169,390

    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)
    nssv187831814e-061276268
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