A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705770



Internal ID129436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22844980..22845477hg38UCSC Ensembl
chr16:22856301..22856798hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145068
Supporting Variants
Samples
Known GenesHS3ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705770
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.072455


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