A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836563



Internal ID22611498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46674620..46676569hg38UCSC Ensembl
chr3:46716110..46718059hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381950
hg191950
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491556
Samples
Known GenesALS2CL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836563
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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