A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091996



Internal ID21278322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124215812..124225184hg38UCSC Ensembl
Innerchr11:124086519..124095889hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg389373
hg199371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116584
Supporting Variants
Samplessample268
Known GenesOR8G2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091996
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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