A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697602



Internal ID121268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85890637..86059713hg38UCSC Ensembl
chr14:86356981..86526057hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38169077
hg19169077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494387
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697602
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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