A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939345



Internal ID26944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136965574..137456000hg38UCSC Ensembl
chr3:136684416..137174842hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38490427
hg19490427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439324
Supporting Variants
Samples
Known GenesIL20RB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939345
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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