A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834306



Internal ID22609241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123087946..123094652hg38UCSC Ensembl
chr3:122806793..122813499hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg386707
hg196707
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484378
Samples
Known GenesPDIA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834306
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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