A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888223



Internal ID22663225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20419596..20419897hg38UCSC Ensembl
chr6:20419827..20420128hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421560
Samples
Known GenesE2F3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888223
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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