A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744696



Internal ID20520697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53469526..53469692hg38UCSC Ensembl
chr20:52086065..52086231hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287272
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744696
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