A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8092n54



Internal ID22775987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34534749..34611054hg38UCSC Ensembl
chr22:34930741..35007046hg19UCSC Ensembl
chr22:33260741..33337046hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3876306
hg1976306
hg1876306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv588943, nsv588944
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8092n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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