A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8082n54



Internal ID22775977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27153180..27179580hg38UCSC Ensembl
chr22:27549141..27575542hg19UCSC Ensembl
chr22:25879141..25905542hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3826401
hg1926402
hg1826402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv588873, nsv588874
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8082n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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