A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100647



Internal ID21279000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61108585..61117970hg38UCSC Ensembl
Innerchr20:59683641..59693026hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg389386
hg199386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114971
Supporting Variants
Samplessample276
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100647
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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