A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989415



Internal ID20556455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15798864..15799323hg38UCSC Ensembl
chr11:15820410..15820869hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989415
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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