A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940925



Internal ID27986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153279712..153322447hg38UCSC Ensembl
chr3:152997501..153040236hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3842736
hg1942736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449295
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940925
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