A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659831



Internal ID21608136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84928527..84928527hg38UCSC Ensembl
chr15:85471758..85471758hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092594
SamplesHG00731
Known GenesSLC28A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659831
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