A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836689



Internal ID22611624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57603037..57611113hg38UCSC Ensembl
chr3:57588764..57596840hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg388077
hg198077
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836689
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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