A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219139



Internal ID20786179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65221590..65221981hg38UCSC Ensembl
chr11:64989061..64989452hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585612
Supporting Variants
Samples
Known GenesSLC22A20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219139
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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