A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936323



Internal ID24945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85382525..85446084hg38UCSC Ensembl
chr3:85431675..85495234hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3863560
hg1963560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443876
Supporting Variants
Samples
Known GenesCADM2, MIR5688
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936323
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