A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665635



Internal ID21613940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50367934..50367934hg38UCSC Ensembl
chr20:48984471..48984471hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116803
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665635
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