A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2467n223



Internal ID22805435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25752451..25753492hg38UCSC Ensembl
chr15:25997598..25998639hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6577042, nsv6591180
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2467n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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