A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12505n54



Internal ID22780400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9793285..9832245hg38UCSC Ensembl
chr9:9793285..9832245hg19UCSC Ensembl
chr9:9783285..9822245hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3838961
hg1938961
hg1838961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613345, nsv613341, nsv613325
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12505n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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