A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696775



Internal ID120441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65163489..65165472hg38UCSC Ensembl
chr14:65630207..65632190hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381984
hg191984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506628
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696775
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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