A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233683



Internal ID20800723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47673799..47675019hg38UCSC Ensembl
chr11:47695351..47696571hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589095
Supporting Variants
Samples
Known GenesAGBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233683
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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