A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452663



Internal ID230809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67035165..67084053hg38UCSC Ensembl
chr3:67085589..67134477hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3848889
hg1948889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452663
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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