A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4678n100



Internal ID20156294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8777359..8816515hg38UCSC Ensembl
chr3:8819045..8858201hg19UCSC Ensembl
chr3:8794045..8833201hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3839157
hg1939157
hg1839157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000284, nsv997573, nsv1012398, nsv997784, nsv997308, nsv1006403, nsv1002818, nsv1014661, nsv1005284
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4678n100
Frequency
Sample Size29084
Observed Gain113
Observed Loss0
Observed Complex0
Frequencyn/a


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