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nsv6467266

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,753

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 38 studies. See in: genome view    
    Submitted genomic54,408,808-54,438,560Question Mark
    Overlapping variant regions from other studies: 145 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):54,802,592-54,832,344Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6467266Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1254,408,80854,438,560
    nsv6467266RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1254,802,59254,832,344

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18188347duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18188347Submitted genomicNC_000012.12:g.544
    08808_54438560dup
    GRCh38 (hg38)NC_000012.12Chr1254,408,80854,438,560
    nssv18188347RemappedPerfectNC_000012.11:g.548
    02592_54832344dup
    GRCh37.p13First PassNC_000012.11Chr1254,802,59254,832,344

    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)
    nssv18188347<0.001139280
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