A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4205n54



Internal ID22772100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20379617..20420298hg38UCSC Ensembl
chr15:20584870..20625551hg19UCSC Ensembl
chr15:18844884..18885565hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3840682
hg1940682
hg1840682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567446, nsv567432, nsv567421, nsv567450, nsv567415
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4205n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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