A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5923112



Internal ID8900515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18993371..19007762hg38UCSC Ensembl
chr8:18850881..18865272hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3814392
hg1914392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659994
Supporting Variants
SamplesHG01359
Known GenesPSD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5923112
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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