A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939470



Internal ID27028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122102871..122102933hg38UCSC Ensembl
chr3:121821718..121821780hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443207
Supporting Variants
Samples
Known GenesCD86
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939470
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.064783


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