A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091809



Internal ID21273247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75972386..76153493hg38UCSC Ensembl
Innerchr11:75683430..75864537hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38181108
hg19181108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116523
Supporting Variants
Samplessample189
Known GenesUVRAG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091809
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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