A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596928



Internal ID20969999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26017802..26017969hg38UCSC Ensembl
chr22:26413768..26413935hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254825
Samples
Known GenesMYO18B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596928
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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