A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5884n100



Internal ID19016252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:257341..447036hg38UCSC Ensembl
chr6:257341..447036hg19UCSC Ensembl
chr6:202341..392036hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38189696
hg19189696
hg18189696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028118, nsv1030962
Samples
Known GenesDUSP22, IRF4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5884n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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