A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12069n54



Internal ID19004245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25212386..25213069hg38UCSC Ensembl
chr8:25069902..25070585hg19UCSC Ensembl
chr8:25125819..25126502hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38684
hg19684
hg18684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610834, nsv610832
Samples
Known GenesDOCK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12069n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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