A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546782



Internal ID20919992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9368610..9370162hg38UCSC Ensembl
chr3:9410294..9411846hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381553
hg191553
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264081
Samples
Known GenesTHUMPD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546782
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