A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1739n54



Internal ID22769634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31373763..31375622hg38UCSC Ensembl
chr11:31395310..31397169hg19UCSC Ensembl
chr11:31351886..31353745hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381860
hg191860
hg181860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553982, nsv553980, nsv553981
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1739n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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