A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5536n54



Internal ID20138960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36107306..36198514hg38UCSC Ensembl
chr17:34434699..34525914hg19UCSC Ensembl
chr17:31458812..31550027hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3891209
hg1991216
hg1891216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574759, nsv574772, nsv574763, nsv574762
Samples
Known GenesCCL3L1, CCL3L3, TBC1D3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5536n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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