A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8086n54



Internal ID20141510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33360843..33364618hg38UCSC Ensembl
chr22:33756829..33760604hg19UCSC Ensembl
chr22:32086829..32090604hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383776
hg193776
hg183776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv588912, nsv588907, nsv588908
Samples
Known GenesLARGE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8086n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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