A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556454



Internal ID15997177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116865227..116867330hg38UCSC Ensembl
Innerchr11:116735943..116738046hg19UCSC Ensembl
Innerchr11:116241153..116243256hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382104
hg192104
hg182104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784599
Samples
Known GenesSIK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556454
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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