A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4169n54



Internal ID22772064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20029080..20428007hg38UCSC Ensembl
chr15:20234333..20633260hg19UCSC Ensembl
chr15:18494347..18893274hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38398928
hg19398928
hg18398928
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567204, nsv567178, nsv567215, nsv567211, nsv567166, nsv567225, nsv567198, nsv567228, nsv567223, nsv567221, nsv567167, nsv567220, nsv567224, nsv567226, nsv567210
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4169n54
Frequency
Sample Size17421
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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