A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654615



Internal ID21602920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2025770..2025770hg38UCSC Ensembl
chr11:2047000..2047000hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382481
hg192481
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074078
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654615
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