A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484316



Internal ID261729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35585617..35588044hg38UCSC Ensembl
chr10:35874545..35876972hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg382428
hg192428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031565
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484316
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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