A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5214n223



Internal ID22808182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28723125..28876752hg38UCSC Ensembl
chr4:28724747..28878374hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38153628
hg19153628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6372306, nsv6364932
Samples
Known GenesMIR4275
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5214n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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