A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614659



Internal ID21562964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158060072..158060072hg38UCSC Ensembl
chr3:157777861..157777861hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129594
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614659
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