A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv266e199



Internal ID20123568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11021769..11049166hg38UCSC Ensembl
chr12:11174368..11201765hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3827398
hg1927398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678172, esv2662894
SamplesHG01498, HG00362
Known GenesPRH1-PRR4, TAS2R19, TAS2R31
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv266e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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