A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251804



Internal ID20818844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34101369..34101814hg38UCSC Ensembl
chr20:32689175..32689620hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598001
Supporting Variants
Samples
Known GenesEIF2S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251804
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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