A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090937



Internal ID21266750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94168845..94176650hg38UCSC Ensembl
Innerchr11:93902011..93909816hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg387806
hg197806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117473
Supporting Variants
Samplessample101
Known GenesPANX1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090937
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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