A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652185



Internal ID21600490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43076800..43076800hg38UCSC Ensembl
chr15:43368998..43368998hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097992
SamplesHG00731
Known GenesUBR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652185
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