A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735753



Internal ID20511696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34228126..34231423hg38UCSC Ensembl
chr20:32815932..32819229hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276803
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735753
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