A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088271



Internal ID21502283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59427635..59427635hg38UCSC Ensembl
chr14:59894353..59894353hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656547
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088271
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