A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627271



Internal ID7014101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92275777..92277897hg38UCSC Ensembl
Innerchr11:92275827..92277847hg38UCSC Ensembl
Outerchr11:92275727..92277947hg38UCSC Ensembl
chr11:92008943..92011063hg19UCSC Ensembl
Innerchr11:92008993..92011013hg19UCSC Ensembl
Outerchr11:92008893..92011113hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg382121
hg192121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14234125
SamplesHG04229
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627271
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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