A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7013n54



Internal ID22774908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114870113..114871246hg38UCSC Ensembl
chr2:115627690..115628823hg19UCSC Ensembl
chr2:115344160..115345293hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381134
hg191134
hg181134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582728, nsv582729
Samples
Known GenesDPP10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7013n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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