A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15114366



Internal ID5116182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103524781..103606409hg38UCSC Ensembl
chr14:103991118..104072746hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3881629
hg1981629
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635599
Supporting Variants
SamplesNA06984
Known GenesAPOPT1, BAG5, TRMT61A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15114366
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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