A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251416



Internal ID20818456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39764436..39764995hg38UCSC Ensembl
chr20:38393078..38393637hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251416
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00037


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