A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695360



Internal ID119026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21722773..21727987hg38UCSC Ensembl
chr14:22191020..22196261hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385215
hg195242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497831
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695360
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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