A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836374



Internal ID22611309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53338952..53349500hg38UCSC Ensembl
chr3:53372979..53383527hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3810549
hg1910549
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493253
Samples
Known GenesDCP1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836374
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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