A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288286



Internal ID20497504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141248525..141248598hg38UCSC Ensembl
chr3:140967367..140967440hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747952
Supporting Variants
Samples
Known GenesACPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288286
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