A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3356n100



Internal ID22789443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:51202320..51242851hg38UCSC Ensembl
chr18:48728690..48769221hg19UCSC Ensembl
chr18:46982688..47023219hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3840532
hg1940532
hg1840532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1067174, nsv1058115, nsv1062925
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)dgv3356n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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