A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451069



Internal ID229256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109413733..109416743hg38UCSC Ensembl
chr3:109132580..109135590hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg383011
hg193011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935380
Samples
Known GenesFLJ25363
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451069
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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