A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3350188



Internal ID15197170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138451952..138452053hg38UCSC Ensembl
Innerchr3:138451970..138452035hg38UCSC Ensembl
Outerchr3:138451934..138452071hg38UCSC Ensembl
chr3:138170794..138170895hg19UCSC Ensembl
Innerchr3:138170812..138170877hg19UCSC Ensembl
Outerchr3:138170776..138170913hg19UCSC Ensembl
chr3:139653484..139653585hg18UCSC Ensembl
Innerchr3:139653502..139653567hg18UCSC Ensembl
Outerchr3:139653466..139653603hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38102
hg19102
hg18102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8671084
SamplesNA19238
Known GenesESYT3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3350188
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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