A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941960



Internal ID21362032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101358101..101358101hg38UCSC Ensembl
chr14:101824438..101824438hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193706
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941960
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