A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364526



Internal ID22590195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10395548..10407421hg38UCSC Ensembl
chr11:10417095..10428968hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811874
hg1911874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916004
Supporting Variants
Samples
Known GenesCAND1.11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364526
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