A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553353



Internal ID16340762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6091627..6096296hg38UCSC Ensembl
Innerchr11:6112857..6117526hg19UCSC Ensembl
Innerchr11:6069433..6074102hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384670
hg194670
hg184670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv766306
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553353
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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