A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642237



Internal ID6682318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36659865..36881208hg38UCSC Ensembl
chr18:34239828..34461171hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38221344
hg19221344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842462
SamplesNA18971
Known GenesFHOD3, KIAA1328, TPGS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642237
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer