A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788787



Internal ID18831435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25291547..25512474hg38UCSC Ensembl
Innerchr22:25687514..25908441hg19UCSC Ensembl
Innerchr22:24017514..24238441hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38220928
hg19220928
hg18220928
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 HumanHap 610
CommentsNumber of probes=59
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788787
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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