A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626149



Internal ID7012983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43665016..43679423hg38UCSC Ensembl
chr11:43686566..43700973hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3814408
hg1914408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14113209
SamplesNA20803
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626149
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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