A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229267



Internal ID20796307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86025119..86025860hg38UCSC Ensembl
chr11:85736161..85736902hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593802
Supporting Variants
Samples
Known GenesPICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229267
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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