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nsv7060175

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,942,873

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8983 SVs from 127 studies. See in: genome view    
    Submitted genomic23,786,777-25,729,649Question Mark
    Overlapping variant regions from other studies: 8985 SVs from 127 studies. See in: genome view    
    Remapped(Score: Perfect):24,031,924-25,974,796Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060175Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1523,786,77725,729,649
    nsv7060175RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1524,031,92425,974,796

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755919inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755919Submitted genomicNC_000015.10:g.237
    86777_25729649inv
    GRCh38 (hg38)NC_000015.10Chr1523,786,77725,729,649
    nssv18755919RemappedPerfectNC_000015.9:g.2403
    1924_25974796inv
    GRCh37.p13First PassNC_000015.9Chr1524,031,92425,974,796

    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)
    nssv187559197e-062276266
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