A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834266



Internal ID22609201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109652867..109685246hg38UCSC Ensembl
chr3:109371714..109404093hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3832380
hg1932380
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834266
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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