A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254376



Internal ID20821416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38362228..38362459hg38UCSC Ensembl
chr20:36990882..36991113hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595630
Supporting Variants
Samples
Known GenesLBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254376
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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