A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741789



Internal ID20517767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38163141..38164538hg38UCSC Ensembl
chr20:36791543..36792940hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381398
hg191398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259837
Samples
Known GenesTGM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741789
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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