A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098326



Internal ID21401683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95319944..95319944hg38UCSC Ensembl
chr14:95786281..95786281hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655709
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098326
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