A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509035



Internal ID285704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102740257..102745024hg38UCSC Ensembl
chr14:103206594..103211361hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384768
hg194768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509035
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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