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nsv6493163

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:707

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 26 studies. See in: genome view    
    Submitted genomic118,064,797-118,065,503Question Mark
    Overlapping variant regions from other studies: 91 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):118,502,602-118,503,308Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6493163Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12118,064,797118,065,503
    nsv6493163RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12118,502,602118,503,308

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17997223deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17997223Submitted genomicNC_000012.12:g.118
    064797_118065503de
    l
    GRCh38 (hg38)NC_000012.12Chr12118,064,797118,065,503
    nssv17997223RemappedPerfectNC_000012.11:g.118
    502602_118503308de
    l
    GRCh37.p13First PassNC_000012.11Chr12118,502,602118,503,308

    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)
    nssv17997223<0.001235482
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