A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2122n54



Internal ID22770017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99437502..99466258hg38UCSC Ensembl
chr11:99308233..99336989hg19UCSC Ensembl
chr11:98813443..98842199hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3828757
hg1928757
hg1828757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556080, nsv556079, nsv556078
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2122n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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