A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992294



Internal ID21901637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188727969..188729805hg38UCSC Ensembl
chr3:188445757..188447593hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381837
hg191837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555893
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992294
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