A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12487n54



Internal ID22780382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5385783..5412546hg38UCSC Ensembl
chr9:5385783..5412546hg19UCSC Ensembl
chr9:5375783..5402546hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3826764
hg1926764
hg1826764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613199, nsv613201
SamplesHGDP00993
Known GenesPLGRKT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12487n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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