A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628169



Internal ID6668313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134353064..134485281hg38UCSC Ensembl
chr11:134222958..134355175hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38132218
hg19132218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14320209
SamplesHG04195
Known GenesB3GAT1, GLB1L2, LOC283177
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628169
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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