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nsv6487696

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:556

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 23 studies. See in: genome view    
    Submitted genomic133,044,643-133,045,198Question Mark
    Overlapping variant regions from other studies: 109 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):133,621,229-133,621,784Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6487696Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12133,044,643133,045,198
    nsv6487696RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,621,229133,621,784

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17999219deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17999219Submitted genomicNC_000012.12:g.133
    044643_133045198de
    l
    GRCh38 (hg38)NC_000012.12Chr12133,044,643133,045,198
    nssv17999219RemappedPerfectNC_000012.11:g.133
    621229_133621784de
    l
    GRCh37.p13First PassNC_000012.11Chr12133,621,229133,621,784

    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)
    nssv17999219<0.0013537804
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