A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024726



Internal ID20591766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48276150..48276782hg38UCSC Ensembl
chr15:48568347..48568979hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502055
Supporting Variants
Samples
Known GenesSLC12A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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