A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746303



Internal ID20522315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117358818..117359141hg38UCSC Ensembl
chr5:116694514..116694837hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746303
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