A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693979



Internal ID117645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23622512..23622579hg38UCSC Ensembl
chr14:24091721..24091788hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693979
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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