A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661360



Internal ID21609665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20853922..20853922hg38UCSC Ensembl
chr12:21006856..21006856hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079148
SamplesHG00732
Known GenesSLCO1B3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661360
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