A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665143



Internal ID9931248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76967910..76968990hg38UCSC Ensembl
chr14:77434253..77435333hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5579235, essv6182028, essv5718487, essv5554765, essv6214626, essv6231977
SamplesNA19466, NA18916, NA19099, NA19360, NA19376, NA19472
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665143
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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