A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7286n100



Internal ID22793373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113364802..113406877hg38UCSC Ensembl
chr8:114377031..114419106hg19UCSC Ensembl
chr8:114446207..114488282hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3842076
hg1942076
hg1842076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031488, nsv1019362
Samples
Known GenesCSMD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7286n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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