A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7517n100



Internal ID20159133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33380150..33468684hg38UCSC Ensembl
chr9:33380148..33468682hg19UCSC Ensembl
chr9:33370148..33458682hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3888535
hg1988535
hg1888535
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024571, nsv1015928
Samples
Known GenesAQP3, AQP7, MIR6851, NOL6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7517n100
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