A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556455



Internal ID16343864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116977613..117082929hg38UCSC Ensembl
Innerchr11:116848329..116953645hg19UCSC Ensembl
Innerchr11:116353539..116458855hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38105317
hg19105317
hg18105317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784600
Samples
Known GenesSIK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556455
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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