A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709389



Internal ID133055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47830900..47839516hg38UCSC Ensembl
chr16:47864811..47873427hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg388617
hg198617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516234
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709389
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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