A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599758



Internal ID20972829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35447655..35448779hg38UCSC Ensembl
chr19:35938557..35939681hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381125
hg191125
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599758
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