A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218096



Internal ID20785136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66941592..66942965hg38UCSC Ensembl
chr11:66709063..66710436hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381374
hg191374
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584719
Supporting Variants
Samples
Known GenesPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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