A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12854n54



Internal ID19005030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113594236..113635117hg38UCSC Ensembl
chr9:116356516..116397397hg19UCSC Ensembl
chr9:115396337..115437218hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3840882
hg1940882
hg1840882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615217, nsv615216
Samples1780862585_A
Known GenesRGS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12854n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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