A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698846



Internal ID122512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101419485..101420703hg38UCSC Ensembl
chr14:101885822..101887040hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381219
hg191219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698846
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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