A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251792



Internal ID20818832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33777390..33778526hg38UCSC Ensembl
chr20:32365196..32366332hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599908
Supporting Variants
Samples
Known GenesZNF341
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251792
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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