A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252194



Internal ID20819234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47650390..47650680hg38UCSC Ensembl
chr20:46279134..46279424hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596273
Supporting Variants
Samples
Known GenesNCOA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252194
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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