A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5378n223



Internal ID22808346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96862601..96870700hg38UCSC Ensembl
chr4:97783752..97791851hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6379826, nsv6388496, nsv6386488, nsv6377488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5378n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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