A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991790



Internal ID21901133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135462385..135464266hg38UCSC Ensembl
chr3:135181227..135183108hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg381882
hg191882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991790
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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