A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555608



Internal ID16343017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83922146..83940059hg38UCSC Ensembl
Innerchr11:83633189..83651102hg19UCSC Ensembl
Innerchr11:83310837..83328750hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3817914
hg1917914
hg1817914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779848
Samples
Known GenesDLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555608
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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