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nsv6923839

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:160

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 25 studies. See in: genome view    
    Submitted genomic119,410,565-119,410,724Question Mark
    Overlapping variant regions from other studies: 91 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):119,848,370-119,848,529Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6923839Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12119,410,565119,410,724
    nsv6923839RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12119,848,370119,848,529

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18593033duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18593033Submitted genomicNC_000012.12:g.119
    410565_119410724du
    p
    GRCh38 (hg38)NC_000012.12Chr12119,410,565119,410,724
    nssv18593033RemappedPerfectNC_000012.11:g.119
    848370_119848529du
    p
    GRCh37.p13First PassNC_000012.11Chr12119,848,370119,848,529

    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)
    nssv18593033<0.001153223540
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