A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12509n54



Internal ID20145933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9801907..9819028hg38UCSC Ensembl
chr9:9801907..9819028hg19UCSC Ensembl
chr9:9791907..9809028hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3817122
hg1917122
hg1817122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613347, nsv613336, nsv613339
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12509n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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