A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092009



Internal ID21278702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:47667508..47680011hg38UCSC Ensembl
Innerchr11:47689060..47701563hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3812504
hg1912504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116422
Supporting Variants
Samplessample273
Known GenesAGBL2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092009
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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