A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693837



Internal ID117503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21150209..21164360hg38UCSC Ensembl
chr14:21618368..21632519hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3814152
hg1914152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497719
Supporting Variants
Samples
Known GenesOR5AU1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693837
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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