A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635297



Internal ID6675410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89618440..89955557hg38UCSC Ensembl
chr14:90084784..90421901hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38337118
hg19337118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15093042, essv15093041, essv15093040
SamplesNA06984, HG01628, HG01345
Known GenesEFCAB11, FOXN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635297
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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