A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023966



Internal ID20591006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42801161..42801318hg38UCSC Ensembl
chr15:43093359..43093516hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495959
Supporting Variants
Samples
Known GenesTTBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03876


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