A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2182n54



Internal ID18994358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108386110..108396128hg38UCSC Ensembl
chr11:108256837..108266855hg19UCSC Ensembl
chr11:107762047..107772065hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3810019
hg1910019
hg1810019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556434, nsv556435, nsv556433
Samples
Known GenesC11orf65
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2182n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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