A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080606



Internal ID21504821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58790184..58790184hg38UCSC Ensembl
chr14:59256902..59256902hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659858
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080606
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