A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5421855



Internal ID9312892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105542622..105545807hg38UCSC Ensembl
Outerchr11:105542585..105545857hg38UCSC Ensembl
Innerchr11:105413349..105416534hg19UCSC Ensembl
Outerchr11:105413312..105416584hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383273
hg193273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658774
Supporting Variants
SamplesNA18502
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5421855
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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