A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639285



Internal ID7026068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80810479..80839928hg38UCSC Ensembl
chr16:80844376..80873825hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3829450
hg1929450
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15534706
SamplesHG01670
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639285
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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