A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251741



Internal ID20818782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32498898..32499461hg38UCSC Ensembl
chr20:31086701..31087264hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597269
Supporting Variants
Samples
Known GenesC20orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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