A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253591



Internal ID20820631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17694612..17695407hg38UCSC Ensembl
chr20:17675257..17676052hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595708
Supporting Variants
Samples
Known GenesBANF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253591
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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