A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666976



Internal ID9933081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97101832..97177760hg38UCSC Ensembl
Outerchr11:97101795..97177810hg38UCSC Ensembl
Innerchr11:96972832..97048760hg19UCSC Ensembl
Outerchr11:96972795..97048810hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3876016
hg1976016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6556966
SamplesNA18912
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666976
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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