A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226440



Internal ID20793480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118277883..118278616hg38UCSC Ensembl
chr11:118148598..118149331hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226440
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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