A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704603



Internal ID128269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11772205..11773800hg38UCSC Ensembl
chr16:11866061..11867656hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381596
hg191596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519699
Supporting Variants
Samples
Known GenesZC3H7A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704603
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.013117


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