A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622049



Internal ID21814096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70402225..70405900hg38UCSC Ensembl
chr18:68069461..68073136hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg383676
hg193676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622049
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