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nsv7040786

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,998

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 31 studies. See in: genome view    
    Submitted genomic33,911,992-33,925,989Question Mark
    Overlapping variant regions from other studies: 119 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):34,377,593-34,391,590Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040786Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr133,911,99233,925,989
    nsv7040786RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr134,377,59334,391,590

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760314inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760314Submitted genomicNC_000001.11:g.339
    11992_33925989inv
    GRCh38 (hg38)NC_000001.11Chr133,911,99233,925,989
    nssv18760314RemappedPerfectNC_000001.10:g.343
    77593_34391590inv
    GRCh37.p13First PassNC_000001.10Chr134,377,59334,391,590

    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)
    nssv187603144e-061276268
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