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nsv6454405

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,451

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 207 SVs from 25 studies. See in: genome view    
    Submitted genomic128,104,617-128,106,067Question Mark
    Overlapping variant regions from other studies: 207 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):129,902,881-129,904,331Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6454405Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10128,104,617128,106,067
    nsv6454405RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10129,902,881129,904,331

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18196776duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18196776Submitted genomicNC_000010.11:g.128
    104617_128106067du
    p
    GRCh38 (hg38)NC_000010.11Chr10128,104,617128,106,067
    nssv18196776RemappedPerfectNC_000010.10:g.129
    902881_129904331du
    p
    GRCh37.p13First PassNC_000010.10Chr10129,902,881129,904,331

    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)
    nssv18196776<0.001139196
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