A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3325n100



Internal ID22789412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22402491..22430278hg38UCSC Ensembl
chr18:19982454..20010241hg19UCSC Ensembl
chr18:18236452..18264239hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3827788
hg1927788
hg1827788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063934, nsv1061451
Samples
Known GenesCTAGE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3325n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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