A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970526



Internal ID22745461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65239955..65239955hg38UCSC Ensembl
chr15:65532293..65532293hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970526
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer