A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671922



Internal ID21620229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51928096..51928096hg38UCSC Ensembl
chr20:50544635..50544635hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116600
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671922
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