A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596300



Internal ID20969371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36255330..36256277hg38UCSC Ensembl
chr21:37627628..37628575hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254698
Samples
Known GenesDOPEY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596300
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