A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255052



Internal ID20822092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43929411..43929726hg38UCSC Ensembl
chr22:44325291..44325606hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597445
Supporting Variants
Samples
Known GenesPNPLA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255052
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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