A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723153



Internal ID146819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37110392..37131811hg38UCSC Ensembl
chr19:37601294..37622713hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3821420
hg1921420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516686
Supporting Variants
Samples
Known GenesZNF420
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723153
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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