A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642236



Internal ID6682317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36659865..36881208hg38UCSC Ensembl
chr18:34239828..34461171hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38221344
hg19221344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842461
SamplesNA12004
Known GenesFHOD3, KIAA1328, TPGS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642236
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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