A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7158n100



Internal ID19017526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28511580..28569458hg38UCSC Ensembl
chr8:28369097..28426975hg19UCSC Ensembl
chr8:28425016..28482894hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3857879
hg1957879
hg1857879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021367, nsv1028651, nsv1033861
Samples
Known GenesFZD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7158n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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