A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525326



Internal ID301491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52529060..52529120hg38UCSC Ensembl
chr15:52821257..52821317hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525326
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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