A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv551e59



Internal ID18986052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2131246..2132244hg38UCSC Ensembl
chr11:2152476..2153474hg19UCSC Ensembl
chr11:2109052..2110050hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3434640, esv3334293
SamplesNA19239, NA19240
Known GenesIGF2, INS-IGF2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv551e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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