A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3672n223



Internal ID22806640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46665601..46671531hg38UCSC Ensembl
chr19:47168858..47174788hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385931
hg195931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6516367, nsv6524373
Samples
Known GenesDACT3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3672n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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