A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698639



Internal ID122305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95386996..95387047hg38UCSC Ensembl
chr14:95853333..95853384hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432986
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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