A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12066n54



Internal ID19004242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25211395..25213015hg38UCSC Ensembl
chr8:25068911..25070531hg19UCSC Ensembl
chr8:25124828..25126448hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381621
hg191621
hg181621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610827, nsv610824, nsv610823, nsv610825
Samples
Known GenesDOCK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12066n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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