A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930314



Internal ID21350383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86298263..86298263hg38UCSC Ensembl
chr15:86841494..86841494hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194626
SamplesHG002
Known GenesAGBL1, AGBL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930314
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer