A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6827n54



Internal ID20140251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43225469..43227728hg38UCSC Ensembl
chr2:43452608..43454867hg19UCSC Ensembl
chr2:43306112..43308371hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg382260
hg192260
hg182260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581651, nsv581650
Samples
Known GenesLINC01126, ZFP36L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6827n54
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