A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834497



Internal ID22609432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107692444..107700768hg38UCSC Ensembl
chr3:107411291..107419615hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg388325
hg198325
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483683, nssv17483684
Samples
Known GenesBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834497
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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