A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12068n54



Internal ID19004244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25211509..25213310hg38UCSC Ensembl
chr8:25069025..25070826hg19UCSC Ensembl
chr8:25124942..25126743hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381802
hg191802
hg181802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610828, nsv610831
Samples
Known GenesDOCK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12068n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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