A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051528



Internal ID102202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127023380..127023829hg38UCSC Ensembl
chr11:126893275..126893724hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051528
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