A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv266e214



Internal ID22756160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:33269209..33351478hg38UCSC Ensembl
chr12:33422144..33504413hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3882270
hg1982270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3629105, esv3629106
SamplesNA19457, HG04029, HG04162, NA19309, NA19321
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv266e214
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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