A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7186n100



Internal ID20158802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42688183..42763570hg38UCSC Ensembl
chr8:42543326..42618713hg19UCSC Ensembl
chr8:42662483..42737870hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3875388
hg1975388
hg1875388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030451, nsv1034121
Samples
Known GenesCHRNA6, CHRNB3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7186n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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