A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5848983



Internal ID8826386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18996083..19001475hg38UCSC Ensembl
chr8:18853593..18858985hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385393
hg195393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676844
Supporting Variants
SamplesNA19438
Known GenesPSD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5848983
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer