A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093198



Internal ID21283651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10291910..10296183hg38UCSC Ensembl
Innerchr11:10313457..10317730hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384274
hg194274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117984
Supporting Variants
Samplessample348
Known GenesSBF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093198
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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