A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228294



Internal ID20795334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47679132..47679947hg38UCSC Ensembl
chr11:47700684..47701499hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579574
Supporting Variants
Samples
Known GenesAGBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228294
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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