A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669907



Internal ID21618212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20458469..20458469hg38UCSC Ensembl
chr20:20439113..20439113hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116239
SamplesNA19238
Known GenesRALGAPA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669907
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