A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635294



Internal ID6675407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89412507..89616461hg38UCSC Ensembl
chr14:89878851..90082805hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38203955
hg19203955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15093031
SamplesNA06984
Known GenesFOXN3, FOXN3-AS1, FOXN3-AS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635294
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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