A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7689n100



Internal ID22793776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93882594..93927045hg38UCSC Ensembl
chr9:96644876..96689327hg19UCSC Ensembl
chr9:95684697..95729148hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3844452
hg1944452
hg1844452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046904, nsv1053137
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)dgv7689n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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