A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15093031



Internal ID5094847
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635294
Supporting Variants
SamplesNA06984
Known GenesFOXN3, FOXN3-AS1, FOXN3-AS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15093031
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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