A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3337192



Internal ID15184180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3173246..3175144hg38UCSC Ensembl
Innerchr11:3174144..3174246hg38UCSC Ensembl
Outerchr11:3172246..3176144hg38UCSC Ensembl
chr11:3194476..3196374hg19UCSC Ensembl
Innerchr11:3195374..3195476hg19UCSC Ensembl
Outerchr11:3193476..3197374hg19UCSC Ensembl
chr11:3151052..3152950hg18UCSC Ensembl
Innerchr11:3152052..3151950hg18UCSC Ensembl
Outerchr11:3150052..3153950hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv553e59
Supporting Variantsessv8688259
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3337192
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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