A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7386n100



Internal ID20159002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6188652..6687205hg38UCSC Ensembl
chr9:6188652..6687205hg19UCSC Ensembl
chr9:6178652..6677205hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38498554
hg19498554
hg18498554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029000, nsv1031459
Samples
Known GenesGLDC, IL33, TPD52L3, UHRF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7386n100
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