A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7489n100



Internal ID22793576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27285644..27305346hg38UCSC Ensembl
chr9:27285642..27305344hg19UCSC Ensembl
chr9:27275642..27295344hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3819703
hg1919703
hg1819703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020039, nsv1020925
Samples
Known GenesEQTN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7489n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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