A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4359n223



Internal ID22807327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5031301..5038400hg38UCSC Ensembl
chr20:5011947..5019046hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6528801, nsv6523283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4359n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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