A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791178



Internal ID18834707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4268493..4422242hg38UCSC Ensembl
Innerchr11:4289723..4443472hg19UCSC Ensembl
Innerchr11:4246299..4400048hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38153750
hg19153750
hg18153750
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891912
Supporting Variants
Samples
Known GenesOR52B4, TRIM21
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=34
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791178
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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