A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091707



Internal ID21270533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33905334..33910303hg38UCSC Ensembl
Innerchr11:33926881..33931850hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384970
hg194970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114484
Supporting Variants
Samplessample152
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091707
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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