A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706992



Internal ID130658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60852686..60853270hg38UCSC Ensembl
chr16:60886590..60887174hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530295
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706992
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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