A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733458



Internal ID20509388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63547749..63547833hg38UCSC Ensembl
chr15:63839948..63840032hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291786
Samples
Known GenesUSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733458
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