A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3439n223



Internal ID22806407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10664270..10665318hg38UCSC Ensembl
chr19:10774946..10775994hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6597842, nsv6596587
Samples
Known GenesILF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3439n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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