A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650052



Internal ID21598357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89567438..89567438hg38UCSC Ensembl
chr14:90033782..90033782hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094421
SamplesHG03125
Known GenesFOXN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650052
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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