A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5534n54



Internal ID20138958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36075679..36109139hg38UCSC Ensembl
chr17:34403039..34436532hg19UCSC Ensembl
chr17:31427152..31460645hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3833461
hg1933494
hg1833494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574757, nsv574756
Samples1780862402_A
Known GenesCCL3, CCL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5534n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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