A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834580



Internal ID22609515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126524075..126529927hg38UCSC Ensembl
chr3:126242918..126248770hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg385853
hg195853
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484435
Samples
Known GenesCHST13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834580
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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