A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218773



Internal ID20785813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65457505..65458544hg38UCSC Ensembl
chr11:65224976..65226015hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381040
hg191040
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579151
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218773
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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