A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1660n54



Internal ID18993836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14358520..14359268hg38UCSC Ensembl
chr11:14380066..14380814hg19UCSC Ensembl
chr11:14336642..14337390hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38749
hg19749
hg18749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553559, nsv553556
Samples
Known GenesRRAS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1660n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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