A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4607n100



Internal ID20156223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18655..244340hg38UCSC Ensembl
chr3:60333..286023hg19UCSC Ensembl
chr3:35333..261023hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38225686
hg19225691
hg18225691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011923, nsv1004245, nsv1005220
Samples
Known GenesCHL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4607n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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