A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255489



Internal ID20822529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29293766..29294377hg38UCSC Ensembl
chr22:29689755..29690366hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597488
Supporting Variants
Samples
Known GenesEWSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255489
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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