A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696460



Internal ID120126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71123713..71129713hg38UCSC Ensembl
chr14:71590430..71596430hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696460
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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