A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7686n100



Internal ID22793773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:84443287..84559247hg38UCSC Ensembl
chr9:87058202..87174162hg19UCSC Ensembl
chr9:86248022..86363982hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38115961
hg19115961
hg18115961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046548, nsv1050777, nsv1050853
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7686n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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