A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7145n100



Internal ID22793232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25116916..25152127hg38UCSC Ensembl
chr8:24974431..25009642hg19UCSC Ensembl
chr8:25030348..25065559hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3835212
hg1935212
hg1835212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020173, nsv1034444, nsv1019493, nsv1023257, nsv1021402
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)dgv7145n100
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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