A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481836



Internal ID259302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117370654..117404870hg38UCSC Ensembl
chr8:118382893..118417109hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg3834217
hg1934217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481836
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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