A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634019



Internal ID21826066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11198990..11610661hg38UCSC Ensembl
chr18:11198989..11610660hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38411672
hg19411672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032021
Supporting Variants
Samples
Known GenesSLC35G4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634019
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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