A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732151



Internal ID155817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35166772..35176647hg38UCSC Ensembl
chr20:33754575..33764450hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg389876
hg199876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516041
Supporting Variants
Samples
Known GenesPROCR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732151
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001562


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