A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556145



Internal ID16343554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102434107..102435784hg38UCSC Ensembl
Innerchr11:102304838..102306515hg19UCSC Ensembl
Innerchr11:101810048..101811725hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381678
hg191678
hg181678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv782012, nssv782013
Samples
Known GenesTMEM123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556145
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