A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12051n54



Internal ID19004227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18998853..19000155hg38UCSC Ensembl
chr8:18856363..18857665hg19UCSC Ensembl
chr8:18900643..18901945hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381303
hg191303
hg181303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610744, nsv610745
Samples
Known GenesPSD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12051n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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