A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554081



Internal ID16341490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39548483..39650724hg38UCSC Ensembl
Innerchr11:39570033..39672274hg19UCSC Ensembl
Innerchr11:39526609..39628850hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38102242
hg19102242
hg18102242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771165
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554081
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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