A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3450145



Internal ID15297093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2433646..2436044hg38UCSC Ensembl
Innerchr11:2434646..2435044hg38UCSC Ensembl
Outerchr11:2432646..2437044hg38UCSC Ensembl
chr11:2454876..2457274hg19UCSC Ensembl
Innerchr11:2455876..2456274hg19UCSC Ensembl
Outerchr11:2453876..2458274hg19UCSC Ensembl
chr11:2411452..2413850hg18UCSC Ensembl
Innerchr11:2412452..2412850hg18UCSC Ensembl
Outerchr11:2410452..2414850hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382399
hg192399
hg182399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688256
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3450145
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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