A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6791n100



Internal ID22792878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:162784..460640hg38UCSC Ensembl
chr8:112784..410640hg19UCSC Ensembl
chr8:102784..400640hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38297857
hg19297857
hg18297857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020182, nsv1017860
Samples
Known GenesFAM87A, FBXO25, OR4F21, RPL23AP53, ZNF596
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6791n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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