A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601328



Internal ID21793375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90314405..90314478hg38UCSC Ensembl
chr13:90966659..90966732hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601328
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer