A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452297



Internal ID230456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26138304..26138859hg38UCSC Ensembl
chr2:26361173..26361728hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16911271
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452297
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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