A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598219



Internal ID20971290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41849267..41850049hg38UCSC Ensembl
chr22:42245271..42246053hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255021
Samples
Known GenesSREBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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