A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506265



Internal ID283016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89963589..89963650hg38UCSC Ensembl
chr14:90429933..90429994hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697164
Samples
Known GenesTDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506265
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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