A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4792n54



Internal ID20138216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101485013..101786434hg38UCSC Ensembl
chr15:102025218..102326637hg19UCSC Ensembl
chr15:99842741..100144160hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38301422
hg19301420
hg18301420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570869, nsv570856, nsv570903, nsv570900, nsv570859, nsv570901, nsv570854, nsv570899, nsv570858
Samples1780862225_A
Known GenesPCSK6, TARSL2, TM2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4792n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer