A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12507n54



Internal ID20145931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9796116..9805134hg38UCSC Ensembl
chr9:9796116..9805134hg19UCSC Ensembl
chr9:9786116..9795134hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg389019
hg199019
hg189019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613329, nsv613328
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12507n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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