A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696456



Internal ID120122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71068623..71068839hg38UCSC Ensembl
chr14:71535340..71535556hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497763
Supporting Variants
Samples
Known GenesPCNX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696456
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.161105


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