A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597388



Internal ID20970459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28852886..28854305hg38UCSC Ensembl
chr22:29248874..29250293hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381420
hg191420
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597388
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