A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3366890



Internal ID15213866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94634908..94634919hg38UCSC Ensembl
Innerchr11:94634910..94634917hg38UCSC Ensembl
Outerchr11:94634899..94634928hg38UCSC Ensembl
chr11:94368074..94368085hg19UCSC Ensembl
Innerchr11:94368076..94368083hg19UCSC Ensembl
Outerchr11:94368065..94368094hg19UCSC Ensembl
chr11:94007722..94007733hg18UCSC Ensembl
Innerchr11:94007731..94007724hg18UCSC Ensembl
Outerchr11:94007713..94007742hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865504
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3366890
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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