A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2511n223



Internal ID22805479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43619301..43636100hg38UCSC Ensembl
chr15:43911499..43928298hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3816800
hg1916800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6506309, nsv6507107
Samples
Known GenesCATSPER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2511n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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