A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834501



Internal ID22609436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109393307..109396236hg38UCSC Ensembl
chr3:109112154..109115083hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg382930
hg192930
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834501
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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