A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837479



Internal ID22612414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97771571..97780106hg38UCSC Ensembl
chr3:97490415..97498950hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg388536
hg198536
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497512
Samples
Known GenesARL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837479
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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