A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3382n100



Internal ID19013750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:66506724..66615886hg38UCSC Ensembl
chr18:64173961..64283123hg19UCSC Ensembl
chr18:62324941..62434103hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38109163
hg19109163
hg18109163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065910, nsv1063783, nsv1067422
Samples
Known GenesCDH19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3382n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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