A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020709



Internal ID21930052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86979558..86980956hg38UCSC Ensembl
chr15:87522789..87524187hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381399
hg191399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613971
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020709
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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