A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3919n54



Internal ID22771814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101457586..101462048hg38UCSC Ensembl
chr14:101923923..101928385hg19UCSC Ensembl
chr14:100993676..100998138hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg384463
hg194463
hg184463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565875, nsv565871
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3919n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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