A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992929



Internal ID21902272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194214969..194216703hg38UCSC Ensembl
chr3:193932758..193934492hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992929
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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