A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090211



Internal ID21286139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14435529..14442268hg38UCSC Ensembl
Innerchr11:14457075..14463814hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg386740
hg196740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117890
Supporting Variants
Samplessample383
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090211
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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