A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5554765



Internal ID9560617
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 StatusS
Merged Variantsesv2665143
Supporting Variants
SamplesNA19099
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5554765
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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