A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543284



Internal ID20916536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52634979..52635571hg38UCSC Ensembl
chr3:52668995..52669587hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260815
Samples
Known GenesPBRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543284
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