A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595984



Internal ID6983302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41873454..42129694hg38UCSC Ensembl
chr3:41914946..42171186hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38256241
hg19256241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10991547
SamplesNA19327
Known GenesTRAK1, ULK4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595984
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer