A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596240



Internal ID20969311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35328598..35329315hg38UCSC Ensembl
chr19:35819501..35820218hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247647
Samples
Known GenesCD22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596240
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