A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254297



Internal ID20821337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23378169..23378603hg38UCSC Ensembl
chr20:23358806..23359240hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598380
Supporting Variants
Samples
Known GenesNAPB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254297
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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