A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv296e214



Internal ID22756190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98297289..98359872hg38UCSC Ensembl
chr12:98691067..98753650hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3862584
hg1962584
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3630505, esv3630506
SamplesNA19917, HG03784, HG03780, HG03771, HG03838, HG01357, HG03870, HG04056
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv296e214
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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