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nsv6477898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58,129

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 754 SVs from 72 studies. See in: genome view    
    Submitted genomic132,427,433-132,485,561Question Mark
    Overlapping variant regions from other studies: 751 SVs from 72 studies. See in: genome view    
    Remapped(Score: Perfect):133,004,019-133,062,147Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6477898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12132,427,433132,485,561
    nsv6477898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,004,019133,062,147

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17999316deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17999316Submitted genomicNC_000012.12:g.132
    427433_132485561de
    l
    GRCh38 (hg38)NC_000012.12Chr12132,427,433132,485,561
    nssv17999316RemappedPerfectNC_000012.11:g.133
    004019_133062147de
    l
    GRCh37.p13First PassNC_000012.11Chr12133,004,019133,062,147

    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)
    nssv17999316<0.001138088
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