A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697368



Internal ID121034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100026381..100026381hg38UCSC Ensembl
chr14:100492718..100492718hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697368
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.092785


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