A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671163



Internal ID21619468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35226721..35226721hg38UCSC Ensembl
chr20:33814524..33814524hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116857
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671163
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