A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3982n54



Internal ID18996158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105167384..105178045hg38UCSC Ensembl
chr14:105633721..105644382hg19UCSC Ensembl
chr14:104704766..104715427hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3810662
hg1910662
hg1810662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566178, nsv566184
Samples
Known GenesJAG2, NUDT14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3982n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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