A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618541



Internal ID21810588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21972855..21973439hg38UCSC Ensembl
chr19:22155657..22156241hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054247
Supporting Variants
Samples
Known GenesZNF208
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618541
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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