A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1661n223



Internal ID22804629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98452766..98454073hg38UCSC Ensembl
chr12:98846544..98847851hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6578019, nsv6593690
Samples
Known GenesSLC9A7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1661n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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