A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3378n100



Internal ID22789465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:64442723..64606186hg38UCSC Ensembl
chr18:62109958..62273421hg19UCSC Ensembl
chr18:60260938..60424401hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38163464
hg19163464
hg18163464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058016, nsv1065121, nsv1055965, nsv1058061, nsv1057778, nsv1067095, nsv1059821
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)dgv3378n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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