A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3396477



Internal ID15243441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169989101..169989427hg38UCSC Ensembl
Innerchr3:169989101..169989427hg38UCSC Ensembl
Outerchr3:169988816..169990000hg38UCSC Ensembl
chr3:169706889..169707215hg19UCSC Ensembl
Innerchr3:169706889..169707215hg19UCSC Ensembl
Outerchr3:169706604..169707788hg19UCSC Ensembl
chr3:171189583..171189909hg18UCSC Ensembl
Innerchr3:171189583..171189909hg18UCSC Ensembl
Outerchr3:171189298..171190482hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38327
hg19327
hg18327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652225
SamplesNA19240
Known GenesSEC62
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3396477
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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