A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8112n54



Internal ID22776007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42313328..42322526hg38UCSC Ensembl
chr22:42709334..42718532hg19UCSC Ensembl
chr22:41039278..41048476hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg389199
hg199199
hg189199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589055, nsv589054
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8112n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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