A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3143n100



Internal ID19013511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36060260..36134107hg38UCSC Ensembl
chr17:34387619..34461489hg19UCSC Ensembl
chr17:31411732..31485602hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3873848
hg1973871
hg1873871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064301, nsv1059828, nsv1065440
Samples
Known GenesCCL18, CCL3, CCL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3143n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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