A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7242n100



Internal ID22793329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75284726..75321984hg38UCSC Ensembl
chr8:76196961..76234219hg19UCSC Ensembl
chr8:76359516..76396774hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3837259
hg1937259
hg1837259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029944, nsv1030122
Samples
Known GenesCASC9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7242n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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