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nsv6491452

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,313

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 387 SVs from 42 studies. See in: genome view    
    Submitted genomic125,983,721-126,149,033Question Mark
    Overlapping variant regions from other studies: 387 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):126,468,267-126,633,579Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6491452Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12125,983,721126,149,033
    nsv6491452RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12126,468,267126,633,579

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17999134deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17999134Submitted genomicNC_000012.12:g.125
    983721_126149033de
    l
    GRCh38 (hg38)NC_000012.12Chr12125,983,721126,149,033
    nssv17999134RemappedPerfectNC_000012.11:g.126
    468267_126633579de
    l
    GRCh37.p13First PassNC_000012.11Chr12126,468,267126,633,579

    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)
    nssv17999134<0.001139252
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