A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956351



Internal ID22731543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143161201..143161201hg38UCSC Ensembl
chr3:142880043..142880043hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956351
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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