A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788114



Internal ID18821519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25311476..25513288hg38UCSC Ensembl
Innerchr22:25707443..25909255hg19UCSC Ensembl
Innerchr22:24037443..24239255hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38201813
hg19201813
hg18201813
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893465
Supporting Variants
Samples
Known GenesCRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=45
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788114
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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