A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519177



Internal ID295533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29566896..29567612hg38UCSC Ensembl
chr19:30057803..30058519hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722661
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519177
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