A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117984



Internal ID21301250
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 StatusM
Merged Variants
Supporting Variantsnssv14093198
Samplessample348
Known GenesSBF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117984
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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