A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv15e198



Internal ID22757747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41282183..41293868hg38UCSC Ensembl
chr18:38862147..38873832hg19UCSC Ensembl
chr18:37116145..37127830hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3811686
hg1911686
hg1811686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2656187, esv2656434
Samples2377 [55], 2242 [59], 2313 [12]
Known Genes
MethodMerging
AnalysisCalls merged from CNV Partition and PennCV algorithms
PlatformMerging
Comments
ReferenceChia_et_al_2012
Pubmed ID23635498
Accession Number(s)dgv15e198
Frequency
Sample Size64
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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