A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5535n54



Internal ID18997711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36104732..36154629hg38UCSC Ensembl
chr17:34432125..34482009hg19UCSC Ensembl
chr17:31456238..31506122hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3849898
hg1949885
hg1849885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574765, nsv574766, nsv574761, nsv574758, nsv574764
Samples
Known GenesCCL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5535n54
Frequency
Sample Size17421
Observed Gain28
Observed Loss0
Observed Complex0
Frequencyn/a


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