A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631308



Internal ID7018117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132670906..132686018hg38UCSC Ensembl
chr12:133247492..133262604hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3815113
hg1915113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14649889
SamplesNA18934
Known GenesPOLE
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631308
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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