A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5188n223



Internal ID22808156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9621107..10087876hg38UCSC Ensembl
chr4:9622731..10089500hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38466770
hg19466770
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6361904, nsv6357145
Samples
Known GenesDRD5, MIR3138, SLC2A9, WDR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5188n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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