A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094421



Internal ID21470343
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 StatusS
Merged Variantsnsv5650052
Supporting Variants
SamplesHG03125
Known GenesFOXN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094421
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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