A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2116n54



Internal ID22770011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99236286..99289771hg38UCSC Ensembl
chr11:99107017..99160502hg19UCSC Ensembl
chr11:98612227..98665712hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3853486
hg1953486
hg1853486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556056, nsv556057
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2116n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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