A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669620



Internal ID9935725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91089703..91175161hg38UCSC Ensembl
Outerchr11:91089666..91175211hg38UCSC Ensembl
Innerchr11:90822871..90908329hg19UCSC Ensembl
Outerchr11:90822834..90908379hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3885546
hg1985546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5849108
SamplesHG00251
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669620
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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