A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834356



Internal ID22609291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146590476..146599956hg38UCSC Ensembl
chr3:146308263..146317743hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg389481
hg199481
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485632
Samples
Known GenesPLSCR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834356
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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