A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551666



Internal ID325101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98277922..98277934hg38UCSC Ensembl
chr13:98930176..98930188hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694113
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551666
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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