A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232240



Internal ID20799280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74992838..74993237hg38UCSC Ensembl
chr11:74703883..74704282hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579652
Supporting Variants
Samples
Known GenesNEU3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232240
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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