A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154690



Internal ID22085195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5864479..5914280hg38UCSC Ensembl
Outerchr11:5862087..5922193hg38UCSC Ensembl
Innerchr11:5885709..5935510hg19UCSC Ensembl
Outerchr11:5883317..5943423hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3860107
hg1960107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv45n97
Supporting Variantsnssv4005713, nssv4005712
Samples
Known GenesOR52E4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154690
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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