A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5067n54



Internal ID22772962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34024926..34218490hg38UCSC Ensembl
chr16:33827393..34020957hg19UCSC Ensembl
chr16:33734894..33928458hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38193565
hg19193565
hg18193565
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572298, nsv572305, nsv572328
Samples
Known GenesLINC00273
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5067n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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