A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3942n54



Internal ID22771837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103521722..103522835hg38UCSC Ensembl
chr14:103988059..103989172hg19UCSC Ensembl
chr14:103057812..103058925hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381114
hg191114
hg181114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566000, nsv566006, nsv566005, nsv566010
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3942n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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