A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1917n54



Internal ID20135341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55602150..55618626hg38UCSC Ensembl
chr11:55369626..55386102hg19UCSC Ensembl
chr11:55126202..55142678hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3816477
hg1916477
hg1816477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554863, nsv554838, nsv554839
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1917n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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