A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227551



Internal ID20794591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38200386..38201085hg38UCSC Ensembl
chr11:38221936..38222635hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227551
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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