A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443512



Internal ID221908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21844391..21867767hg38UCSC Ensembl
chr3:21885883..21909259hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3823377
hg1923377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443512
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