A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944879



Internal ID30587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188015075..188017049hg38UCSC Ensembl
chr3:187732863..187734837hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381975
hg191975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944879
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.101311


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