A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5854193



Internal ID8831596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133089774..133090727hg38UCSC Ensembl
Outerchr11:133089617..133090880hg38UCSC Ensembl
Innerchr11:132959669..132960622hg19UCSC Ensembl
Outerchr11:132959512..132960775hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677127
Supporting Variants
SamplesNA19726
Known GenesOPCML
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5854193
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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