A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656467



Internal ID21604772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17214564..17214564hg38UCSC Ensembl
chr11:17236111..17236111hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073797
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656467
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