A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409281



Internal ID22467151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140902265..140903515hg38UCSC Ensembl
chr3:140621107..140622357hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381251
hg191251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896196
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409281
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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