A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084742



Internal ID21511464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69361931..69361931hg38UCSC Ensembl
chr16:69395834..69395834hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653890
Supporting Variants
SamplesNA24385
Known GenesTERF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084742
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