A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251699



Internal ID20818739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30692739..30700986hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251699
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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