A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072832



Internal ID21501713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116797649..116802971hg38UCSC Ensembl
chr11:116668365..116673687hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385323
hg195323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590888
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072832
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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