A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986036



Internal ID20553076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103800498..103801016hg38UCSC Ensembl
chr11:103671226..103671744hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457061
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986036
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00096


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