A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253792



Internal ID20820832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40356515..40357271hg38UCSC Ensembl
chr22:40752519..40753275hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598686
Supporting Variants
Samples
Known GenesADSL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253792
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00046


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