A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253805



Internal ID20820845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40625571..40626168hg38UCSC Ensembl
chr22:41021575..41022172hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596655
Supporting Variants
Samples
Known GenesMKL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253805
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer