A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7085n100



Internal ID22793172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13176688..13226060hg38UCSC Ensembl
chr8:13034197..13083569hg19UCSC Ensembl
chr8:13078568..13127940hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3849373
hg1949373
hg1849373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019346, nsv1019729
Samples
Known GenesDLC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7085n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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