A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986906



Internal ID20553946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114315168..114324127hg38UCSC Ensembl
chr11:114185890..114194849hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg388960
hg198960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468148
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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