A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7668n100



Internal ID20159284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69381047..69564931hg38UCSC Ensembl
chr9:71995963..72179847hg19UCSC Ensembl
chr9:71185783..71369667hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38183885
hg19183885
hg18183885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035633, nsv1048650
Samples
Known GenesAPBA1, FAM189A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7668n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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