A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236758



Internal ID20803798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102734949..102752720hg38UCSC Ensembl
chr11:102605680..102623451hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3817772
hg1917772
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584293
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236758
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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