A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656763



Internal ID21605068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111246742..111246742hg38UCSC Ensembl
chr11:111117467..111117467hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072505
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656763
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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