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nsv6785170

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:216,547

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 610 SVs from 74 studies. See in: genome view    
    Submitted genomic29,105,952-29,322,498Question Mark
    Overlapping variant regions from other studies: 610 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):29,073,729-29,290,275Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6785170Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr629,105,95229,322,498
    nsv6785170RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr629,073,72929,290,275

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18524443deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18524443Submitted genomicNC_000006.12:g.291
    05952_29322498del
    GRCh38 (hg38)NC_000006.12Chr629,105,95229,322,498
    nssv18524443RemappedPerfectNC_000006.11:g.290
    73729_29290275del
    GRCh37.p13First PassNC_000006.11Chr629,073,72929,290,275

    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)
    nssv185244431.1e-053275050
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