A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834836



Internal ID22609771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113823109..113833264hg38UCSC Ensembl
chr3:113541956..113552111hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3810156
hg1910156
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834836
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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