A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5241n100



Internal ID19015609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67374315..67472988hg38UCSC Ensembl
chr4:68240033..68338706hg19UCSC Ensembl
chr4:67922628..68021301hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3898674
hg1998674
hg1898674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013936, nsv1000928
Samples
Known GenesCENPC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5241n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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