A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3659n54



Internal ID22771554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41130185..41209263hg38UCSC Ensembl
chr14:41599390..41678466hg19UCSC Ensembl
chr14:40669140..40748216hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3879079
hg1979077
hg1879077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564477, nsv564483, nsv564494, nsv564484, nsv564478, nsv564511, nsv564480, nsv564474, nsv564508, nsv564472, nsv564473, nsv564509, nsv564475, nsv564496, nsv564479, nsv564499, nsv564498, nsv564482, nsv564495
Samples
Known GenesLOC644919
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3659n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss183
Observed Complex0
Frequencyn/a


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