A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835471



Internal ID22610406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186203436..186205467hg38UCSC Ensembl
chr3:185921225..185923256hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg382032
hg192032
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489758
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835471
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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