A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2715111



Internal ID5062401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89213464..89213560hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv6858134
SamplesSSM087
Known GenesACSF3
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2715111
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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