A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720601



Internal ID144267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3602028..3602916hg38UCSC Ensembl
chr19:3602026..3602914hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526388
Supporting Variants
Samples
Known GenesTBXA2R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720601
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000938


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