A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3487n223



Internal ID22806455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23405769..23882455hg38UCSC Ensembl
chr19:23588571..24065257hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38476687
hg19476687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6598216, nsv6596313
Samples
Known GenesRPSAP58, ZNF675, ZNF681
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3487n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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