A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15535514



Internal ID5920653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80918206..80938218hg38UCSC Ensembl
chr16:80952103..80972115hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3820013
hg1920013
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639298
Supporting Variants
SamplesNA19331
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15535514
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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