A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596647



Internal ID20969718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42008040..42008414hg38UCSC Ensembl
chr19:42512192..42512566hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246299
Samples
Known GenesGRIK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596647
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