A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255122



Internal ID20822162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31886798..31888290hg38UCSC Ensembl
chr22:32282784..32284276hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381493
hg191493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596926
Supporting Variants
Samples
Known GenesDEPDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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