A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255189



Internal ID20822229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34658595..34659126hg38UCSC Ensembl
chr22:35054587..35055118hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255189
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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