A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737223



Internal ID20513182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39315751..39315811hg38UCSC Ensembl
chr13:39889888..39889948hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737223
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