A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659662



Internal ID21607967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91308550..91308550hg38UCSC Ensembl
chr15:91851780..91851780hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084550
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659662
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