A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744938



Internal ID20520942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160019921..160019980hg38UCSC Ensembl
chr3:159737708..159737767hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282616
Samples
Known GenesIL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744938
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