A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5397n223



Internal ID22808365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106248301..106265000hg38UCSC Ensembl
chr4:107169458..107186157hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3816700
hg1916700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6377841, nsv6393971
Samples
Known GenesTBCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5397n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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