A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv453n21



Internal ID18990926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25398068..25408410hg38UCSC Ensembl
chr8:25255584..25265926hg19UCSC Ensembl
chr8:25311501..25321843hg18UCSC Ensembl
chr8:25311501..25321843hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3810343
hg1910343
hg1810343
hg1710343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519361, nsv526195
Samples
Known GenesDOCK5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv453n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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