A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091111



Internal ID21290029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65475355..65497936hg38UCSC Ensembl
Innerchr11:65242826..65265407hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3822582
hg1922582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112369
Supporting Variants
Samplessample54
Known GenesMALAT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091111
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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