A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4772n223



Internal ID22807740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4098929..4113074hg38UCSC Ensembl
chr3:4140613..4154758hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3814146
hg1914146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6364701, nsv6365814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4772n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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