A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5480764



Internal ID9477016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86296527..86301067hg38UCSC Ensembl
chr11:86007569..86012109hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg384541
hg194541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667718
Supporting Variants
SamplesNA18948
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5480764
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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