A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967290



Internal ID45504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80188110..80202053hg38UCSC Ensembl
chr5:79483932..79497872hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3813944
hg1913941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464696
Supporting Variants
Samples
Known GenesSERINC5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967290
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