A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2659n223



Internal ID22805627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1225888..1244940hg38UCSC Ensembl
chr16:1275888..1294941hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819053
hg1919054
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6581153, nsv6584494
Samples
Known GenesTPSAB1, TPSB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2659n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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