A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497949



Internal ID274962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74451744..74453770hg38UCSC Ensembl
chr14:74918447..74920473hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382027
hg192027
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497949
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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