A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236865



Internal ID20803905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66102983..66106446hg38UCSC Ensembl
chr11:65870454..65873917hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383464
hg193464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576433
Supporting Variants
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236865
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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