A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836194



Internal ID22611129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39876734..39885795hg38UCSC Ensembl
chr3:39918225..39927286hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg389062
hg199062
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491467
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836194
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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