A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101487



Internal ID21284419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32670347..32677669hg38UCSC Ensembl
Innerchr19:33161253..33168575hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg387323
hg197323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115322
Supporting Variants
Samplessample360
Known GenesANKRD27, RGS9BP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101487
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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