A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154748



Internal ID22085253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79272928..79282708hg38UCSC Ensembl
Outerchr11:79270153..79290404hg38UCSC Ensembl
Innerchr11:78983973..78993753hg19UCSC Ensembl
Outerchr11:78981198..79001449hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3820252
hg1920252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007202
Samples
Known GenesTENM4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154748
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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