A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218741



Internal ID20785781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43462927..43464242hg38UCSC Ensembl
chr11:43484477..43485792hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577291
Supporting Variants
Samples
Known GenesTTC17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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