A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3501n223



Internal ID22806469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36256501..36259200hg38UCSC Ensembl
chr19:36747403..36750102hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6516608, nsv6527362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3501n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer