A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12928n54



Internal ID20146352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133078923..133167883hg38UCSC Ensembl
chr9:135954310..136043270hg19UCSC Ensembl
chr9:134944131..135033091hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3888961
hg1988961
hg1888961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615606, nsv615608, nsv615611
Samples
Known GenesCELP, GBGT1, RALGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12928n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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