A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv286n172



Internal ID22814660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81866423..81866745hg38UCSC Ensembl
chr16:81900028..81900350hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4432381, nsv4432380
SamplesMDQ045, SMI041
Known GenesPLCG2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv286n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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