A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990964



Internal ID21900307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11166623..11166861hg38UCSC Ensembl
chr3:11208309..11208547hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527039
Samples
Known GenesHRH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990964
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