A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101623



Internal ID20668663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66170039..66172180hg38UCSC Ensembl
chr3:66155714..66157855hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382142
hg192142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362951
Supporting Variants
Samples
Known GenesSLC25A26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101623
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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