A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618901



Internal ID21810948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54984321..54994165hg38UCSC Ensembl
chr18:52651552..52661396hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg389845
hg199845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618901
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