A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252490



Internal ID20819530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35388133..35388928hg38UCSC Ensembl
chr20:33975936..33976731hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596809
Supporting Variants
Samples
Known GenesUQCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252490
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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