A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790311



Internal ID18812882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134299300..134339014hg38UCSC Ensembl
Innerchr11:134169194..134208908hg19UCSC Ensembl
Innerchr11:133674404..133714118hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3839715
hg1939715
hg1839715
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892113
Supporting Variants
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790311
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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