A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1939n223



Internal ID22804907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82613701..82627800hg38UCSC Ensembl
chr13:83187836..83201935hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3814100
hg1914100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6483080, nsv6475732, nsv6492434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1939n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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