A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958253



Internal ID22733327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16236104..16236104hg38UCSC Ensembl
chr3:16277611..16277611hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958253
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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