A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556288



Internal ID16343697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107368380..107369763hg38UCSC Ensembl
Innerchr11:107239106..107240489hg19UCSC Ensembl
Innerchr11:106744316..106745699hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381384
hg191384
hg181384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2162n54
Supporting Variantsnssv783735, nssv783736
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556288
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