A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497548



Internal ID274578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98033984..98034054hg38UCSC Ensembl
chr12:98427762..98427832hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497548
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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