A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv979n223



Internal ID22803947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18246623..18268275hg38UCSC Ensembl
chr11:18268170..18289822hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821653
hg1921653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6582218, nsv6592985
Samples
Known GenesSAA1, SAA2, SAA2-SAA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv979n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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