A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4608n100



Internal ID20156224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18655..438490hg38UCSC Ensembl
chr3:60333..480173hg19UCSC Ensembl
chr3:35333..455173hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38419836
hg19419841
hg18419841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010433, nsv1008604
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)dgv4608n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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