A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890478



Internal ID22665506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32470086..32470194hg38UCSC Ensembl
chr3:32511578..32511686hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890478
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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