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nsv6394708

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:550,081

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2044 SVs from 100 studies. See in: genome view    
    Submitted genomic62,719,218-63,269,298Question Mark
    Overlapping variant regions from other studies: 2044 SVs from 100 studies. See in: genome view    
    Remapped(Score: Perfect):63,584,936-64,135,016Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6394708Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr462,719,21863,269,298
    nsv6394708RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr463,584,93664,135,016

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18210928duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18210928Submitted genomicNC_000004.12:g.627
    19218_63269298dup
    GRCh38 (hg38)NC_000004.12Chr462,719,21863,269,298
    nssv18210928RemappedPerfectNC_000004.11:g.635
    84936_64135016dup
    GRCh37.p13First PassNC_000004.11Chr463,584,93664,135,016

    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)
    nssv18210928<0.001539078
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