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nsv6367386

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:662

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 19 studies. See in: genome view    
    Submitted genomic21,841,381-21,842,042Question Mark
    Overlapping variant regions from other studies: 118 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):21,843,004-21,843,665Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6367386Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr421,841,38121,842,042
    nsv6367386RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr421,843,00421,843,665

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18116113deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18116113Submitted genomicNC_000004.12:g.218
    41381_21842042del
    GRCh38 (hg38)NC_000004.12Chr421,841,38121,842,042
    nssv18116113RemappedPerfectNC_000004.11:g.218
    43004_21843665del
    GRCh37.p13First PassNC_000004.11Chr421,843,00421,843,665

    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)
    nssv18116113<0.001438466
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