A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899550



Internal ID22674681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99327644..99332495hg38UCSC Ensembl
chr3:99046488..99051339hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg384852
hg194852
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899550
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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