A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3389376



Internal ID14889657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2427946..2429844hg38UCSC Ensembl
Innerchr11:2428844..2428946hg38UCSC Ensembl
Outerchr11:2426946..2430844hg38UCSC Ensembl
chr11:2449176..2451074hg19UCSC Ensembl
Innerchr11:2450074..2450176hg19UCSC Ensembl
Outerchr11:2448176..2452074hg19UCSC Ensembl
chr11:2405752..2407650hg18UCSC Ensembl
Innerchr11:2406752..2406650hg18UCSC Ensembl
Outerchr11:2404752..2408650hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688250
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3389376
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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