A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7728n54



Internal ID20141152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10416793..10813996hg38UCSC Ensembl
chr21:10698461..11095664hg19UCSC Ensembl
chr21:9720332..10117535hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38397204
hg19397204
hg18397204
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586887, nsv586888, nsv586898, nsv586886, nsv586885
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7728n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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