A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658228



Internal ID21606533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72290279..72290279hg38UCSC Ensembl
chr15:72582620..72582620hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082430
SamplesHG00733
Known GenesCELF6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658228
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