A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989316



Internal ID20556356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21588801..21693800hg38UCSC Ensembl
chr11:21610347..21715346hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38105000
hg19105000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989316
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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