A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073067



Internal ID21490056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123808260..123811090hg38UCSC Ensembl
chr11:123678968..123681798hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382831
hg192831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585690
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073067
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