A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561397



Internal ID20934468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120729530..120765086hg38UCSC Ensembl
chr3:120448377..120483933hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3835557
hg1935557
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261776
Samples
Known GenesGTF2E1, RABL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561397
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