A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627642



Internal ID7014470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107070173..107331876hg38UCSC Ensembl
chr11:106940899..107202602hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38261704
hg19261704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14274437, essv14274434, essv14274436, essv14274435
SamplesHG02360, HG03782, HG03742, HG03755
Known GenesCWF19L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627642
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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