A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv660e59



Internal ID22761880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70025098..70026596hg38UCSC Ensembl
chr11:69871204..69872702hg19UCSC Ensembl
chr11:69548852..69550350hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3411474, esv3366102
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv660e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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