A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv971n223



Internal ID22803939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9350376..9353493hg38UCSC Ensembl
chr11:9371923..9375040hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383118
hg193118
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6589431, nsv6592099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv971n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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