A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627114



Internal ID7013944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87068041..87192374hg38UCSC Ensembl
chr11:86779083..86903416hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38124334
hg19124334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14223526
SamplesHG02085
Known GenesTMEM135
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627114
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer