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nsv7067078

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:890,249

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2234 SVs from 84 studies. See in: genome view    
    Submitted genomic65,167,217-66,057,465Question Mark
    Overlapping variant regions from other studies: 2234 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):65,633,935-66,524,183Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067078Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1465,167,21766,057,465
    nsv7067078RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,633,93566,524,183

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753932inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753932Submitted genomicNC_000014.9:g.6516
    7217_66057465inv
    GRCh38 (hg38)NC_000014.9Chr1465,167,21766,057,465
    nssv18753932RemappedPerfectNC_000014.8:g.6563
    3935_66524183inv
    GRCh37.p13First PassNC_000014.8Chr1465,633,93566,524,183

    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)
    nssv187539324e-061276268
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