A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625955



Internal ID21818002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50944509..50949971hg38UCSC Ensembl
chr18:48470879..48476341hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg385463
hg195463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025836
Supporting Variants
Samples
Known GenesME2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625955
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