A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100738



Internal ID21283954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21392977..21395787hg38UCSC Ensembl
Innerchr20:21373615..21376425hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114815
Supporting Variants
Samplessample353
Known GenesNKX2-4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100738
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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