A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836361



Internal ID22611296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50012512..50018442hg38UCSC Ensembl
chr3:50049945..50055875hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385931
hg195931
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493190
Samples
Known GenesRBM6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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