A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3779n223



Internal ID22806747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197016..763147hg38UCSC Ensembl
chr2:197016..763147hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38566132
hg19566132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6325759, nsv6317336
Samples
Known GenesACP1, FAM150B, SH3YL1, TMEM18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3779n223
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