A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2502n223



Internal ID22805470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38069501..38075000hg38UCSC Ensembl
chr15:38361702..38367201hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6497631, nsv6507933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2502n223
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