A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438096



Internal ID216667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13291071..13297868hg38UCSC Ensembl
chr3:13332571..13339368hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386798
hg196798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438096
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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