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nsv6589693

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:882

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 78 SVs from 24 studies. See in: genome view    
    Submitted genomic110,455,220-110,456,101Question Mark
    Overlapping variant regions from other studies: 78 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):110,893,025-110,893,906Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6589693Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12110,455,220110,456,101
    nsv6589693RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12110,893,025110,893,906

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18219045inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18219045Submitted genomicNC_000012.12:g.110
    455220_110456101in
    v
    GRCh38 (hg38)NC_000012.12Chr12110,455,220110,456,101
    nssv18219045RemappedPerfectNC_000012.11:g.110
    893025_110893906in
    v
    GRCh37.p13First PassNC_000012.11Chr12110,893,025110,893,906

    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)
    nssv18219045<0.001136424
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