A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980499



Internal ID21889842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108023641..108023703hg38UCSC Ensembl
chr1:108566263..108566325hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980499
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