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nsv7059107

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56,737

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 452 SVs from 54 studies. See in: genome view    
    Submitted genomic19,193,470-19,250,206Question Mark
    Overlapping variant regions from other studies: 458 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):19,193,468-19,250,204Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059107Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr919,193,47019,250,206
    nsv7059107RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr919,193,46819,250,204

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785796inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785796Submitted genomicNC_000009.12:g.191
    93470_19250206inv
    GRCh38 (hg38)NC_000009.12Chr919,193,47019,250,206
    nssv18785796RemappedPerfectNC_000009.11:g.191
    93468_19250204inv
    GRCh37.p13First PassNC_000009.11Chr919,193,46819,250,204

    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)
    nssv187857964e-061276268
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