A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8093n54



Internal ID20141517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36137894..36187036hg38UCSC Ensembl
chr22:36533942..36583084hg19UCSC Ensembl
chr22:34863888..34913030hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3849143
hg1949143
hg1849143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv588950, nsv588951, nsv588952
Samples
Known GenesAPOL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8093n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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