A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779854



Internal ID16073810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84623101..84830360hg38UCSC Ensembl
Innerchr11:84334144..84541403hg19UCSC Ensembl
Innerchr11:84011792..84219051hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38207260
hg19207260
hg18207260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555615
Supporting Variants
Samples
Known GenesDLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv779854
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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