A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654519



Internal ID21602824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36661642..36661642hg38UCSC Ensembl
chr19:37152544..37152544hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383153
hg193153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105149
SamplesNA19239
Known GenesZNF461
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654519
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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