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nsv7047564

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,593

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 244 SVs from 42 studies. See in: genome view    
    Submitted genomic34,046,692-34,072,284Question Mark
    Overlapping variant regions from other studies: 244 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):34,271,759-34,297,351Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047564Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr234,046,69234,072,284
    nsv7047564RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr234,271,75934,297,351

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768468inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768468Submitted genomicNC_000002.12:g.340
    46692_34072284inv
    GRCh38 (hg38)NC_000002.12Chr234,046,69234,072,284
    nssv18768468RemappedPerfectNC_000002.11:g.342
    71759_34297351inv
    GRCh37.p13First PassNC_000002.11Chr234,271,75934,297,351

    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)
    nssv187684683.2e-059274540
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