A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052213



Internal ID102661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119026083..119026935hg38UCSC Ensembl
chr11:118896793..118897645hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503195
Supporting Variants
Samples
Known GenesSLC37A4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052213
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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