A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697669



Internal ID121335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89015310..89015560hg38UCSC Ensembl
chr14:89481654..89481904hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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