A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533655



Internal ID309540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17797076..17797164hg38UCSC Ensembl
chr19:17907885..17907973hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721979
Samples
Known GenesB3GNT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533655
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