A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553792



Internal ID16341201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24413656..24430480hg38UCSC Ensembl
Innerchr11:24435202..24452026hg19UCSC Ensembl
Innerchr11:24391778..24408602hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3816825
hg1916825
hg1816825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1703n54
Supporting Variantsnssv768986, nssv768987
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553792
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