A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365293



Internal ID22590962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22933144..22959871hg38UCSC Ensembl
chr10:23222073..23248800hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3826728
hg1926728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921206
Supporting Variants
Samples
Known GenesARMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365293
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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