A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784587



Internal ID15731857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116865227..116866122hg38UCSC Ensembl
Innerchr11:116735943..116736838hg19UCSC Ensembl
Innerchr11:116241153..116242048hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38896
hg19896
hg18896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556452
Supporting Variants
Samples
Known GenesSIK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv784587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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