A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083709



Internal ID21503617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55518237..55518237hg38UCSC Ensembl
chr16:55552149..55552149hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg386087
hg196087
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649658
Supporting Variants
SamplesNA19239
Known GenesLPCAT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083709
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