A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892102



Internal ID19186498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116506908..116541896hg38UCSC Ensembl
Outerchr11:116506908..116541896hg38UCSC Ensembl
Innerchr11:116377625..116412613hg19UCSC Ensembl
Outerchr11:116377625..116412613hg19UCSC Ensembl
Innerchr11:115882835..115917823hg18UCSC Ensembl
Outerchr11:115882835..115917823hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3834989
hg1934989
hg1834989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792866
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892102
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer