A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4328n223



Internal ID22807296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241823601..242006600hg38UCSC Ensembl
chr2:242765757..242948751hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38183000
hg19182995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6353286, nsv6353254
Samples
Known GenesCXXC11, PDCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4328n223
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