A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723334



Internal ID147000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39409499..39412022hg38UCSC Ensembl
chr19:39900139..39902662hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382524
hg192524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528258
Supporting Variants
Samples
Known GenesMIR4530
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723334
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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