A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836626



Internal ID22611561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:54234746..54256851hg38UCSC Ensembl
chr3:54268773..54290878hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3822106
hg1922106
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493271
Samples
Known GenesCACNA2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836626
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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