A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5691298



Internal ID8668701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106725141..106725438hg38UCSC Ensembl
chr11:106595867..106596164hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663324
Supporting Variants
SamplesNA12249
Known GenesGUCY1A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5691298
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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