A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252845



Internal ID20819885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10451167..10451687hg38UCSC Ensembl
chr20:10431815..10432335hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598029
Supporting Variants
Samples
Known GenesSLX4IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252845
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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