A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499395



Internal ID276369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51436828..51436959hg38UCSC Ensembl
chr14:51903546..51903677hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499395
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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