A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3358n100



Internal ID22789445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53815447..53896009hg38UCSC Ensembl
chr18:51341817..51422379hg19UCSC Ensembl
chr18:49595815..49676377hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3880563
hg1980563
hg1880563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067388, nsv1058867
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3358n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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