A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111858



Internal ID21295124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33845049..33851252hg38UCSC Ensembl
Innerchr11:33866595..33872798hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg386204
hg196204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090076, nssv14093236
Samplessample41, sample364
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111858
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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