A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12234n54



Internal ID20145658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88588522..89717279hg38UCSC Ensembl
chr8:89600751..90729507hg19UCSC Ensembl
chr8:89669867..90798629hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381128758
hg191128757
hg181128763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611713, nsv611714
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12234n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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