A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834747



Internal ID22609682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16500118..16502850hg38UCSC Ensembl
chr3:16541625..16544357hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382733
hg192733
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487027
Samples
Known GenesRFTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834747
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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