A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116574



Internal ID21299840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:35222398..35237594hg38UCSC Ensembl
Innerchr11:35243945..35259141hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3815197
hg1915197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv198n145
Supporting Variantsnssv14090267, nssv14090905, nssv14090204
Samplessample90, sample380, sample400
Known GenesCD44
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116574
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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