A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506108



Internal ID282862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63571070..63577627hg38UCSC Ensembl
chr14:64037788..64044345hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg386558
hg196558
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506108
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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