A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671937



Internal ID9591356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11019460..11075113hg38UCSC Ensembl
chr12:11172059..11227712hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3855654
hg1955654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv265e199
Supporting Variantsessv6331641, essv6102923, essv6374653
SamplesNA12058, HG00693, HG00258
Known GenesPRH1-PRR4, TAS2R19, TAS2R31, TAS2R46
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671937
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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