A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660822



Internal ID9580241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11014775..11069972hg38UCSC Ensembl
chr12:11167374..11222571hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3855198
hg1955198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv265e199
Supporting Variantsessv5885464
SamplesHG00133
Known GenesPRH1-PRR4, TAS2R19, TAS2R31, TAS2R46
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660822
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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