A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091070



Internal ID21270273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130067688..130074120hg38UCSC Ensembl
Innerchr11:129937583..129944015hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg386433
hg196433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114584
Supporting Variants
Samplessample149
Known GenesAPLP2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091070
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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