A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7696n100



Internal ID22793783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104597521..104609842hg38UCSC Ensembl
chr9:107359802..107372123hg19UCSC Ensembl
chr9:106399623..106411944hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3812322
hg1912322
hg1812322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045875, nsv1036979
Samples
Known GenesOR13C2, OR13C5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7696n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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