A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12516n54



Internal ID22780411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10075721..10102903hg38UCSC Ensembl
chr9:10075721..10102903hg19UCSC Ensembl
chr9:10065721..10092903hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3827183
hg1927183
hg1827183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613371, nsv613372
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12516n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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