A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482874



Internal ID260319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90090111..90096222hg38UCSC Ensembl
chr8:91102339..91108450hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg386112
hg196112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482874
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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