A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3369075



Internal ID15216051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146279856..146279875hg38UCSC Ensembl
Innerchr3:146279852..146279879hg38UCSC Ensembl
Outerchr3:146279833..146279898hg38UCSC Ensembl
chr3:145997643..145997662hg19UCSC Ensembl
Innerchr3:145997639..145997666hg19UCSC Ensembl
Outerchr3:145997620..145997685hg19UCSC Ensembl
chr3:147480333..147480352hg18UCSC Ensembl
Innerchr3:147480356..147480329hg18UCSC Ensembl
Outerchr3:147480310..147480375hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9612169
SamplesNA19143
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3369075
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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