A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249336



Internal ID20816376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223822171..223822516hg38UCSC Ensembl
chr1:224009873..224010218hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538050
Supporting Variants
Samples
Known GenesTP53BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249336
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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