A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228116



Internal ID20795156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117150858..117151297hg38UCSC Ensembl
chr11:117021574..117022013hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583388
Supporting Variants
Samples
Known GenesPAFAH1B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228116
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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