A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495879



Internal ID272975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99642776..99643292hg38UCSC Ensembl
chr14:100109113..100109629hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495879
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