A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255167



Internal ID20822207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33843907..33844738hg38UCSC Ensembl
chr22:34239895..34240726hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595873
Supporting Variants
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255167
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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