A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992290



Internal ID21901633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188142580..188142643hg38UCSC Ensembl
chr3:187860368..187860431hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992290
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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