A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708671



Internal ID132337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77854684..77926098hg38UCSC Ensembl
chr16:77888581..77959995hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3871415
hg1971415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524342
Supporting Variants
Samples
Known GenesVAT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708671
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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