A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688533



Internal ID15044633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94664738..94666336hg38UCSC Ensembl
Innerchr11:94665336..94665738hg38UCSC Ensembl
Outerchr11:94663738..94667336hg38UCSC Ensembl
chr11:94397904..94399502hg19UCSC Ensembl
Innerchr11:94398502..94398904hg19UCSC Ensembl
Outerchr11:94396904..94400502hg19UCSC Ensembl
chr11:94037552..94039150hg18UCSC Ensembl
Innerchr11:94038552..94038150hg18UCSC Ensembl
Outerchr11:94036552..94040150hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3356576
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688533
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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