A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697981



Internal ID121647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76828691..76828737hg38UCSC Ensembl
chr14:77295034..77295080hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422532
Supporting Variants
Samples
Known GenesC14orf166B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697981
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0064


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