A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614294



Internal ID21806341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77066411..77066411hg38UCSC Ensembl
chr15:77358753..77358753hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382372
hg192372
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081276
Supporting Variants
Samples
Known GenesTSPAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614294
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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