A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722172



Internal ID145838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20092360..20212851hg38UCSC Ensembl
chr19:20203169..20323660hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38120492
hg19120492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524547
Supporting Variants
Samples
Known GenesZNF486, ZNF90
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722172
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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