A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930939



Internal ID21351009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68866111..68866111hg38UCSC Ensembl
chr14:69332828..69332828hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382148
hg192148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194445
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930939
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer