A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662082



Internal ID9928187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38719065..38807289hg38UCSC Ensembl
Outerchr11:38718997..38807351hg38UCSC Ensembl
Innerchr11:38740615..38828839hg19UCSC Ensembl
Outerchr11:38740547..38828901hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3888355
hg1988355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6173407
SamplesHG00614
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662082
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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