A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627644



Internal ID7014472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107257370..107361314hg38UCSC Ensembl
chr11:107128096..107232040hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38103945
hg19103945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14274453, essv14274452, essv14274451
SamplesHG03782, HG03742, HG03755
Known GenesCWF19L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627644
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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