A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3407372



Internal ID14907648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133901747..133902645hg38UCSC Ensembl
Innerchr11:133901746..133902646hg38UCSC Ensembl
Outerchr11:133900747..133903645hg38UCSC Ensembl
chr11:133771642..133772540hg19UCSC Ensembl
Innerchr11:133771641..133772541hg19UCSC Ensembl
Outerchr11:133770642..133773540hg19UCSC Ensembl
chr11:133276852..133277750hg18UCSC Ensembl
Innerchr11:133277751..133276851hg18UCSC Ensembl
Outerchr11:133275852..133278750hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv727e59
Supporting Variantsessv8688207
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3407372
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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