A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2773n54



Internal ID18994949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89708316..89709574hg38UCSC Ensembl
chr12:90102093..90103351hg19UCSC Ensembl
chr12:88626224..88627482hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg381259
hg191259
hg181259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv559708, nsv559713, nsv559712, nsv559706
Samples
Known GenesLINC00936
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2773n54
Frequency
Sample Size17421
Observed Gain20
Observed Loss0
Observed Complex0
Frequencyn/a


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