A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666007



Internal ID21614312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35446991..35446991hg38UCSC Ensembl
chr20:34034801..34034801hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116859
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666007
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