A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598393



Internal ID20971464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17523326..17524388hg38UCSC Ensembl
chr22:18002354..18003435hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381063
hg191082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254880
Samples
Known GenesCECR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598393
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