A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230081



Internal ID20797121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14391336..14393550hg38UCSC Ensembl
chr11:14412882..14415096hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382215
hg192215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590168
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230081
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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