A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627088



Internal ID6667236
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14221785, essv14221786, essv14221787
SamplesHG00626, HG02085, HG00864
Known GenesME3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627088
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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