A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12275n54



Internal ID22780170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113857336..113896246hg38UCSC Ensembl
chr8:114869565..114908475hg19UCSC Ensembl
chr8:114938741..114977651hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3838911
hg1938911
hg1838911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611960, nsv611959
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12275n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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