A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053661



Internal ID103615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124037303..124050752hg38UCSC Ensembl
chr11:123908010..123921459hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3813450
hg1913450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513552
Supporting Variants
Samples
Known GenesOR10G7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053661
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002967


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