A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14274434



Internal ID2665641
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627642
Supporting Variants
SamplesHG02360
Known GenesCWF19L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14274434
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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