A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2362n223



Internal ID22805330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:17013701..17018400hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6510482, nsv6507842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2362n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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