A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5172n223



Internal ID22808140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9362901..9458700hg38UCSC Ensembl
chr4:9364627..9460426hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3895800
hg1995800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6362426, nsv6370365
Samples
Known GenesDEFB131, USP17L24, USP17L25, USP17L26, USP17L27, USP17L28, USP17L29, USP17L30, USP17L5, USP17L6P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5172n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer