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nsv6937226

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,316

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 368 SVs from 42 studies. See in: genome view    
    Submitted genomic125,983,721-126,149,036Question Mark
    Overlapping variant regions from other studies: 368 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):126,468,267-126,633,582Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6937226Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12125,983,721126,149,036
    nsv6937226RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12126,468,267126,633,582

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18356009deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18356009Submitted genomicNC_000012.12:g.125
    983721_126149036de
    l
    GRCh38 (hg38)NC_000012.12Chr12125,983,721126,149,036
    nssv18356009RemappedPerfectNC_000012.11:g.126
    468267_126633582de
    l
    GRCh37.p13First PassNC_000012.11Chr12126,468,267126,633,582

    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)
    nssv183560091.4e-054275978
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