A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789241



Internal ID19168372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98113646..98294667hg38UCSC Ensembl
Innerchr11:97984374..98165395hg19UCSC Ensembl
Innerchr11:97489584..97670605hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38181022
hg19181022
hg18181022
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892085
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789241
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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