A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv779852



Internal ID16073808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84511394..84704079hg38UCSC Ensembl
Innerchr11:84222437..84415122hg19UCSC Ensembl
Innerchr11:83900085..84092770hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38192686
hg19192686
hg18192686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555612
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)nssv779852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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