A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599851



Internal ID20972922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19247743..19248179hg38UCSC Ensembl
chr22:19235266..19235702hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254918
Samples
Known GenesCLTCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599851
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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