A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2532n223



Internal ID22805500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49140039..49141437hg38UCSC Ensembl
chr15:49432236..49433634hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381399
hg191399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6581404, nsv6595270
Samples
Known GenesCOPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2532n223
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