A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920028



Internal ID22695251
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 StatusM
Merged Variants
Supporting Variantsnssv17359187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920028
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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