A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14221786



Internal ID4223602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86468825..86593258hg38UCSC Ensembl
chr11:86179867..86304300hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38124434
hg19124434
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627088
Supporting Variants
SamplesHG00864
Known GenesME3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14221786
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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