A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236516



Internal ID20803556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9522776..9523990hg38UCSC Ensembl
chr11:9544323..9545537hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585536
Supporting Variants
Samples
Known GenesZNF143
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236516
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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