A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932307



Internal ID22261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40479895..40486976hg38UCSC Ensembl
chr3:40521386..40528467hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg387082
hg197082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437137
Supporting Variants
Samples
Known GenesZNF619
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932307
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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