A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251729



Internal ID20818770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32180754..32183149hg38UCSC Ensembl
chr20:30768557..30770952hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg382396
hg192396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595695
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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