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nsv6554206

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,198

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 24 studies. See in: genome view    
    Submitted genomic50,832,510-50,842,707Question Mark
    Overlapping variant regions from other studies: 115 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):49,449,047-49,459,244Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6554206Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2050,832,51050,842,707
    nsv6554206RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2049,449,04749,459,244

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18205279duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18205279Submitted genomicNC_000020.11:g.508
    32510_50842707dup
    GRCh38 (hg38)NC_000020.11Chr2050,832,51050,842,707
    nssv18205279RemappedPerfectNC_000020.10:g.494
    49047_49459244dup
    GRCh37.p13First PassNC_000020.10Chr2049,449,04749,459,244

    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)
    nssv18205279<0.001139286
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