A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2162n54



Internal ID22770057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107368380..107369767hg38UCSC Ensembl
chr11:107239106..107240493hg19UCSC Ensembl
chr11:106744316..106745703hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381388
hg191388
hg181388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556289, nsv556288
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2162n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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