A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12852n54



Internal ID22780747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112953875..112983376hg38UCSC Ensembl
chr9:115716155..115745656hg19UCSC Ensembl
chr9:114755976..114785477hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3829502
hg1929502
hg1829502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615202, nsv615200
SamplesNINDS_232
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12852n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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