A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553280



Internal ID16340689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5738876..5740095hg38UCSC Ensembl
Innerchr11:5760106..5761325hg19UCSC Ensembl
Innerchr11:5716682..5717901hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381220
hg191220
hg181220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1609n54
Supporting Variantsnssv765579
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553280
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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