A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223599



Internal ID20790640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3789195..3789377hg38UCSC Ensembl
chr11:3810425..3810607hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591029
Supporting Variants
Samples
Known GenesNUP98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223599
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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