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nsv6974060

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,691

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 383 SVs from 63 studies. See in: genome view    
    Submitted genomic85,976,605-86,006,295Question Mark
    Overlapping variant regions from other studies: 383 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):86,442,949-86,472,639Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6974060Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1485,976,60586,006,295
    nsv6974060RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1486,442,94986,472,639

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18391497deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18391497Submitted genomicNC_000014.9:g.8597
    6605_86006295del
    GRCh38 (hg38)NC_000014.9Chr1485,976,60586,006,295
    nssv18391497RemappedPerfectNC_000014.8:g.8644
    2949_86472639del
    GRCh37.p13First PassNC_000014.8Chr1486,442,94986,472,639

    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)
    nssv183914974e-061276208
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