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nsv6494435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 166 SVs from 36 studies. See in: genome view    
    Submitted genomic132,692,234-132,692,334Question Mark
    Overlapping variant regions from other studies: 166 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):133,268,820-133,268,920Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6494435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12132,692,234132,692,334
    nsv6494435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,268,820133,268,920

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17999326deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17999326Submitted genomicNC_000012.12:g.132
    692234_132692334de
    l
    GRCh38 (hg38)NC_000012.12Chr12132,692,234132,692,334
    nssv17999326RemappedPerfectNC_000012.11:g.133
    268820_133268920de
    l
    GRCh37.p13First PassNC_000012.11Chr12133,268,820133,268,920

    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)
    nssv17999326<0.001126406
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