A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114971



Internal ID21298237
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 StatusM
Merged Variants
Supporting Variantsnssv14100647
Samplessample276
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114971
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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