A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7149n100



Internal ID22793236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25536638..25552325hg38UCSC Ensembl
chr8:25394154..25409841hg19UCSC Ensembl
chr8:25450071..25465758hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3815688
hg1915688
hg1815688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024712, nsv1024022, nsv1029657
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)dgv7149n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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