A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986194



Internal ID20553235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105640635..105726797hg38UCSC Ensembl
chr11:105511362..105597523hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3886163
hg1986162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456971
Supporting Variants
Samples
Known GenesGRIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986194
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