A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1037n223



Internal ID22804005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47736256..47737679hg38UCSC Ensembl
chr11:47757808..47759231hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381424
hg191424
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6591194, nsv6591503
Samples
Known GenesFNBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1037n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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