A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599433



Internal ID21548067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3717945..3718912hg38UCSC Ensembl
chr19:3717943..3718910hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105160
SamplesNA19239
Known GenesTJP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599433
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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