A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661152



Internal ID9580571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:749209..753048hg38UCSC Ensembl
Outerchr11:749052..753201hg38UCSC Ensembl
Innerchr11:749209..753048hg19UCSC Ensembl
Outerchr11:749052..753201hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384150
hg194150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6523656, essv6252607, essv6291232
SamplesHG00500, NA19057, NA18637
Known GenesTALDO1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661152
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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