A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723118



Internal ID146784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36632408..36871986hg38UCSC Ensembl
chr19:37123310..37362888hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38239579
hg19239579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528459
Supporting Variants
Samples
Known GenesZNF345, ZNF461, ZNF567, ZNF790, ZNF790-AS1, ZNF850
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723118
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer