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nsv7060547

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:244,205

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 612 SVs from 65 studies. See in: genome view    
    Submitted genomic35,282,974-35,527,178Question Mark
    Overlapping variant regions from other studies: 619 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):35,282,971-35,527,175Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060547Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr935,282,97435,527,178
    nsv7060547RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr935,282,97135,527,175

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783920inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783920Submitted genomicNC_000009.12:g.352
    82974_35527178inv
    GRCh38 (hg38)NC_000009.12Chr935,282,97435,527,178
    nssv18783920RemappedPerfectNC_000009.11:g.352
    82971_35527175inv
    GRCh37.p13First PassNC_000009.11Chr935,282,97135,527,175

    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)
    nssv187839207e-062276268
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