A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986348



Internal ID20553388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108239882..108240403hg38UCSC Ensembl
chr11:108110609..108111130hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467085
Supporting Variants
Samples
Known GenesATM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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