A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709874



Internal ID133540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81805264..81816106hg38UCSC Ensembl
chr16:81838869..81849711hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3810843
hg1910843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532616
Supporting Variants
Samples
Known GenesPLCG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709874
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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