A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553279



Internal ID16340688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5738230..5740096hg38UCSC Ensembl
Innerchr11:5759460..5761326hg19UCSC Ensembl
Innerchr11:5716036..5717902hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381867
hg191867
hg181867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1608n54
Supporting Variantsnssv765578
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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