A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905977



Internal ID22681171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41898654..42136014hg38UCSC Ensembl
chr3:41940146..42177506hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38237361
hg19237361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417897
Samples
Known GenesTRAK1, ULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905977
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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