A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940877



Internal ID27953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150038559..150038647hg38UCSC Ensembl
chr3:149756346..149756434hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940877
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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