A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697566



Internal ID121232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85352824..85352879hg38UCSC Ensembl
chr14:85819168..85819223hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506981
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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