A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099964



Internal ID21276003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:43697091..43745000hg38UCSC Ensembl
Innerchr20:42325731..42373640hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3847910
hg1947910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116387
Supporting Variants
Samplessample231
Known GenesGTSF1L, MYBL2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099964
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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