A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3943n54



Internal ID22771838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103521722..103523420hg38UCSC Ensembl
chr14:103988059..103989757hg19UCSC Ensembl
chr14:103057812..103059510hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566001, nsv566011, nsv566002, nsv566007
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3943n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer