A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788984



Internal ID18822353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21960940..22145879hg38UCSC Ensembl
Innerchr22:22315312..22500272hg19UCSC Ensembl
Innerchr22:20645312..20830272hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38184940
hg19184961
hg18184961
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893445
Supporting Variants
Samples
Known GenesTOP3B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=116
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788984
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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