A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738039



Internal ID20514005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32563104..32563734hg38UCSC Ensembl
chr20:31150906..31151536hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285835
Samples
Known GenesC20orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738039
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer