A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892106



Internal ID22667151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25485517..25487475hg38UCSC Ensembl
chr3:25527008..25528966hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381959
hg191959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426094
Samples
Known GenesRARB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892106
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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