A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695359



Internal ID119025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21720590..21721308hg38UCSC Ensembl
chr14:22188831..22189555hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38719
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498137
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695359
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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