A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3333n100



Internal ID20154949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32901167..32960383hg38UCSC Ensembl
chr18:30481131..30540347hg19UCSC Ensembl
chr18:28735129..28794345hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3859217
hg1959217
hg1859217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056985, nsv1060448
Samples
Known GenesCCDC178
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3333n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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