A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4296n223



Internal ID22807264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:227376001..227393657hg38UCSC Ensembl
chr2:228240717..228258373hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3817657
hg1917657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6354773, nsv6347595
Samples
Known GenesTM4SF20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4296n223
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