A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234331



Internal ID20801372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14890132..14890561hg38UCSC Ensembl
chr11:14911678..14912107hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580060
Supporting Variants
Samples
Known GenesCYP2R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234331
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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