A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8266n54



Internal ID22776161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26381978..26397924hg38UCSC Ensembl
chr3:26423469..26439415hg19UCSC Ensembl
chr3:26398473..26414419hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3815947
hg1915947
hg1815947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589971, nsv589970, nsv589968, nsv589969
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8266n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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