A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7464n223



Internal ID22810432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113010301..113036700hg38UCSC Ensembl
chr8:114022530..114048929hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3826400
hg1926400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6430874, nsv6416086, nsv6424457
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7464n223
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