A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653515



Internal ID21601820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39519562..39519562hg38UCSC Ensembl
chr15:39811763..39811763hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086059
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653515
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