A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288038



Internal ID20497256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25839556..25839641hg38UCSC Ensembl
chr3:25881047..25881132hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288038
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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