A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8125n54



Internal ID22776020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47322927..47391141hg38UCSC Ensembl
chr22:47718677..47786891hg19UCSC Ensembl
chr22:46097341..46165555hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3868215
hg1968215
hg1868215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589144, nsv589143
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8125n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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