A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5184n223



Internal ID22808152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9575444..10681382hg38UCSC Ensembl
chr4:9577068..10683006hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381105939
hg191105939
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6360762, nsv6356685
Samples
Known GenesCLNK, DRD5, MIR3138, SLC2A9, WDR1, ZNF518B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5184n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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