A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087509



Internal ID21464552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22618936..22618936hg38UCSC Ensembl
chr14:23087839..23087839hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649656
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087509
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