A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4188n54



Internal ID22772083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20354526..20424722hg38UCSC Ensembl
chr15:20559779..20629975hg19UCSC Ensembl
chr15:18819793..18889989hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3870197
hg1970197
hg1870197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567342, nsv567345
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4188n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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