A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6788n100



Internal ID22792875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96386..302856hg38UCSC Ensembl
chr8:46386..252856hg19UCSC Ensembl
chr8:36386..242856hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38206471
hg19206471
hg18206471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034372, nsv1022117, nsv1035050
Samples
Known GenesOR4F21, 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)dgv6788n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer