A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2187n54



Internal ID22770082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122687294..122741587hg38UCSC Ensembl
chr11:122558002..122612295hg19UCSC Ensembl
chr11:122063212..122117505hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3854294
hg1954294
hg1854294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556480, nsv556479
SamplesHGDP00995, HGDP01019
Known GenesUBASH3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2187n54
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