A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796835



Internal ID18828646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33532063..33554551hg38UCSC Ensembl
Innerchr22:33928049..33950537hg19UCSC Ensembl
Innerchr22:32258049..32280537hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3822489
hg1922489
hg1822489
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893477
Supporting Variants
Samples
Known GenesLARGE
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796835
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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