A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359187



Internal ID22584856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116497264..116497412hg38UCSC Ensembl
chr11:116367981..116368129hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359187
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