A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1523n54



Internal ID18993699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:557342..656940hg38UCSC Ensembl
chr11:557342..656940hg19UCSC Ensembl
chr11:547342..646940hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3899599
hg1999599
hg1899599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552859, nsv552857
Samples
Known GenesC11orf35, CDHR5, DEAF1, DRD4, IRF7, LOC143666, MIR210, MIR210HG, PHRF1, RASSF7, SCT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1523n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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