A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7157n100



Internal ID19017525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28499087..28584581hg38UCSC Ensembl
chr8:28356604..28442098hg19UCSC Ensembl
chr8:28412523..28498017hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3885495
hg1985495
hg1885495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030130, nsv1030449, nsv1017667, nsv1020526
Samples
Known GenesFZD3, MIR4288
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7157n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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