A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663501



Internal ID9929606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22474175..22487263hg38UCSC Ensembl
chr18:20054138..20067226hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3813089
hg1913089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6154195, essv6311575, essv5566250, essv5914424, essv6104648
SamplesNA18923, NA18874, NA18867, NA19452, NA19713
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663501
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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