A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6792n100



Internal ID22792879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:285367..467709hg38UCSC Ensembl
chr8:235367..417709hg19UCSC Ensembl
chr8:225367..407709hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38182343
hg19182343
hg18182343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016901, nsv1028103
Samples
Known GenesFAM87A, FBXO25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6792n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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