A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3388n100



Internal ID22789475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67896823..67992425hg38UCSC Ensembl
chr18:65564060..65659662hg19UCSC Ensembl
chr18:63715040..63810642hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3895603
hg1995603
hg1895603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060354, nsv1061406
Samples
Known GenesLOC643542
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3388n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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