A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639319



Internal ID21587624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22293639..22293639hg38UCSC Ensembl
chr6:22293868..22293868hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151747
SamplesHG00513
Known GenesPRL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639319
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