A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4351n223



Internal ID22807319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:726662..930692hg38UCSC Ensembl
chr20:707306..911335hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38204031
hg19204030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6532514, nsv6525596
Samples
Known GenesANGPT4, FAM110A, SLC52A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4351n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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