A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3967n54



Internal ID20137391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104864865..104865985hg38UCSC Ensembl
chr14:105331202..105332322hg19UCSC Ensembl
chr14:104402247..104403367hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381121
hg191121
hg181121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566111, nsv566113, nsv566114, nsv566112, nsv566118
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3967n54
Frequency
Sample Size17421
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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