A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619159



Internal ID21567464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11297197..11297197hg38UCSC Ensembl
chrY:13452873..13452873hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg381006
hg191006
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169723
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619159
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