A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8569n54



Internal ID22776464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128661277..128700211hg38UCSC Ensembl
chr3:128380120..128419054hg19UCSC Ensembl
chr3:129862810..129901744hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3838935
hg1938935
hg1838935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591615, nsv591616, nsv591610, nsv591619, nsv591613, nsv591612, nsv591609, nsv591621, nsv591611, nsv591614
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8569n54
Frequency
Sample Size17421
Observed Gain52
Observed Loss0
Observed Complex0
Frequencyn/a


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