A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929299



Internal ID20249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4130659..4271913hg38UCSC Ensembl
chr3:4172343..4313597hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38141255
hg19141255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929299
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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