A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7685n100



Internal ID22793772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80304115..80461286hg38UCSC Ensembl
chr9:82919030..83076201hg19UCSC Ensembl
chr9:82108850..82266021hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38157172
hg19157172
hg18157172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047075, nsv1042238
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)dgv7685n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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