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nsv7076165

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,709

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 180 SVs from 29 studies. See in: genome view    
    Submitted genomic35,785,665-35,793,373Question Mark
    Overlapping variant regions from other studies: 187 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):35,785,662-35,793,370Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076165Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr935,785,66535,793,373
    nsv7076165RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr935,785,66235,793,370

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783928inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783928Submitted genomicNC_000009.12:g.357
    85665_35793373inv
    GRCh38 (hg38)NC_000009.12Chr935,785,66535,793,373
    nssv18783928RemappedPerfectNC_000009.11:g.357
    85662_35793370inv
    GRCh37.p13First PassNC_000009.11Chr935,785,66235,793,370

    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)
    nssv187839284e-061276268
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