A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3066n100



Internal ID19013434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89067685..89301626hg38UCSC Ensembl
chr16:89134093..89368034hg19UCSC Ensembl
chr16:87661594..87895535hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38233942
hg19233942
hg18233942
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056030, nsv1061607, nsv1062213
Samples
Known GenesACSF3, ANKRD11, CDH15, LINC00304, LOC400558, SLC22A31, ZNF778
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3066n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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