A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090220



Internal ID21286322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14813490..14821236hg38UCSC Ensembl
Innerchr11:14835036..14842782hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg387747
hg197747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110429
Supporting Variants
Samplessample386
Known GenesPDE3B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090220
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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