A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588050



Internal ID21536611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56444439..56444604hg38UCSC Ensembl
chr19:56955808..56955973hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106413
SamplesNA19239
Known GenesZNF667
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588050
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