A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231523



Internal ID20798563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20386186..20386796hg38UCSC Ensembl
chr11:20407732..20408342hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231523
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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