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nsv6478161

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:483

    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 genomic133,058,144-133,058,626Question Mark
    Overlapping variant regions from other studies: 109 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):133,634,730-133,635,212Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6478161Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12133,058,144133,058,626
    nsv6478161RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12133,634,730133,635,212

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17999222deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17999222Submitted genomicNC_000012.12:g.133
    058144_133058626de
    l
    GRCh38 (hg38)NC_000012.12Chr12133,058,144133,058,626
    nssv17999222RemappedPerfectNC_000012.11:g.133
    634730_133635212de
    l
    GRCh37.p13First PassNC_000012.11Chr12133,634,730133,635,212

    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)
    nssv17999222<0.001639192
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