A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952172



Internal ID21372242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95293374..95293374hg38UCSC Ensembl
chr14:95759711..95759711hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194518
SamplesHG002
Known GenesCLMN
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952172
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