A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110684



Internal ID21293950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:35222398..35236822hg38UCSC Ensembl
Innerchr11:35243945..35258369hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3814425
hg1914425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv198n145
Supporting Variantsnssv14090308
Samplessample420
Known GenesCD44
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110684
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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